Difference between revisions of "Sandybox"

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(Tag: 2017 source edit)
(Tag: 2017 source edit)
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ICD-10-CM-Chapter 16
+
ICD-10-CM-Chapter 17
  
Certain conditions originating in the perinatal period (P00-P96)
+
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  
 
Note  
 
Note  
  
Codes from this chapter are for use on newborn records only, never on maternal records  
+
Codes from this chapter are not for use on maternal records  
  
''Includes''  
+
''Excludes2''  
 +
 
 +
inborn errors of metabolism (E70-E88)
  
conditions that have their origin in the fetal or perinatal period (before birth through the first 28 days after birth)
+
This chapter contains the following blocks
  
even if morbidity occurs later
+
*'''[[Q00-Q07]]'''
  
''Excludes2''
+
Congenital malformations of the nervous system
  
congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
+
*'''[[Q10-Q18]]'''
  
endocrine, nutritional and metabolic diseases (E00-E88)
+
Congenital malformations of eye, ear, face and neck
  
injury, poisoning and certain other consequences of external causes (S00-T88)
+
*'''[[Q20-Q28]]'''
  
neoplasms (C00-D49)
+
Congenital malformations of the circulatory system
  
tetanus neonatorum (A33)
+
*'''[[Q30-Q34]]'''
  
This chapter contains the following blocks
+
Congenital malformations of the respiratory system
  
*'''[[P00-P04]]'''
+
*'''[[Q35-Q37]]'''
  
Newborn affected by maternal factors and by complications of pregnancy, labor, and delivery
+
Cleft lip and cleft palate
  
*'''[[P05-P08]]'''
+
*'''[[Q38-Q45]]'''
  
Disorders of newborn related to length of gestation and fetal growth
+
Other congenital malformations of the digestive system
  
*'''[[P09]]'''
+
*'''[[Q50-Q56]]'''
  
Abnormal findings on neonatal screening
+
Congenital malformations of genital organs
  
*'''[[P10-P15]]'''
+
*'''[[Q60-Q64]]'''
  
Birth trauma
+
Congenital malformations of the urinary system
  
*'''[[P19-P29]]'''
+
*'''[[Q65-Q79]]'''
  
Respiratory and cardiovascular disorders specific to the perinatal period
+
Congenital malformations and deformations of the musculoskeletal system
  
*'''[[P35-P39]]'''
+
*'''[[Q80-Q89]]'''
  
Infections specific to the perinatal period
+
Other congenital malformations
  
*'''[[P50-P61]]'''
+
*'''[[Q90-Q99]]'''
  
Hemorrhagic and hematological disorders of newborn
+
Chromosomal abnormalities, not elsewhere classified
  
*'''[[P70-P74]]'''
+
Congenital malformations of the nervous system (Q00-Q07)
  
Transitory endocrine and metabolic disorders specific to newborn
+
*'''[[Q00]]''' Anencephaly and similar malformations
  
*'''[[P76-P78]]'''
+
*'''[[Q00.0]]''' Anencephaly
  
Digestive system disorders of newborn
+
Acephaly
  
*'''[[P80-P83]]'''
+
Acrania
  
Conditions involving the integument and temperature regulation of newborn
+
Amyelencephaly
  
*'''[[P84]]'''
+
Hemianencephaly
  
Other problems with newborn
+
Hemicephaly
  
*'''[[P90-P96]]'''
+
*'''[[Q00.1]]''' Craniorachischisis
  
Other disorders originating in the perinatal period
+
*'''[[Q00.2]]''' Iniencephaly
  
Newborn affected by maternal factors and by complications of pregnancy, labor, and delivery (P00-P04)
+
*'''[[Q01]]''' Encephalocele
  
Note
+
''Includes''
  
These codes are for use when the listed maternal conditions are specified as the cause of confirmed morbidity or
+
Arnold-Chiari syndrome, type III
  
potential morbidity which have their origin in the perinatal period (before birth through the first 28 days after
+
encephalocystocele
  
birth)
+
encephalomyelocele
  
*'''[[P00]]''' Newborn affected by maternal conditions that may be unrelated to present pregnancy ''Code first''
+
hydroencephalocele
  
any current condition in newborn
+
hydromeningocele, cranial
  
''Excludes2''
+
meningocele, cerebral
  
encounter for observation of newborn for suspected diseases and conditions ruled out (Z05.-)
+
meningoencephalocele
  
newborn affected by maternal complications of pregnancy (P01.-)
+
''Excludes1''
  
newborn affected by maternal endocrine and metabolic disorders (P70-P74)  
+
Meckel-Gruber syndrome (Q61.9)
  
newborn affected by noxious substances transmitted via placenta or breast milk (P04.-)
+
*'''[[Q01.0]]''' Frontal encephalocele
  
*'''[[P00.0]]''' Newborn affected by maternal hypertensive disorders
+
*'''[[Q01.1]]''' Nasofrontal encephalocele
  
Newborn affected by maternal conditions classifiable to O10-O11, O13-O16
+
*'''[[Q01.2]]''' Occipital encephalocele
  
*'''[[P00.1]]''' Newborn affected by maternal renal and urinary tract diseases
+
*'''[[Q01.8]]''' Encephalocele of other sites
  
Newborn affected by maternal conditions classifiable to N00-N39
+
*'''[[Q01.9]]''' Encephalocele, unspecified
  
*'''[[P00.2]]''' Newborn affected by maternal infectious and parasitic diseases
+
*'''[[Q02]]''' Microcephaly
  
Newborn affected by maternal infectious disease classifiable to A00-B99, J09 and J10
+
''Includes''
  
''Excludes1''
+
hydromicrocephaly
  
maternal genital tract or other localized infections (P00.8)
+
micrencephalon ''Code first''
  
''Excludes2''
+
, if applicable, congenital Zika virus disease
  
infections specific to the perinatal period (P35-P39)
+
''Excludes1''
  
*'''[[P00.3]]''' Newborn affected by other maternal circulatory and respiratory diseases
+
Meckel-Gruber syndrome (Q61.9)
  
Newborn affected by maternal conditions classifiable to I00-I99, J00-J99, Q20-Q34 and not included in P00.0,
+
*'''[[Q03]]''' Congenital hydrocephalus
  
*'''[[P00.2]]'''
+
''Includes''  
  
*'''[[P00.4]]''' Newborn affected by maternal nutritional disorders
+
hydrocephalus in newborn
  
Newborn affected by maternal disorders classifiable to E40-E64
+
''Excludes1''
  
Maternal malnutrition NOS
+
Arnold-Chiari syndrome, type II (Q07.0-)
  
*'''[[P00.5]]''' Newborn affected by maternal injury
+
acquired hydrocephalus (G91.-)
  
Newborn affected by maternal conditions classifiable to O9A.2-
+
hydrocephalus due to congenital toxoplasmosis (P37.1)
  
*'''[[P00.6]]''' Newborn affected by surgical procedure on mother
+
hydrocephalus with spina bifida (Q05.0-Q05.4)
  
Newborn affected by amniocentesis
+
*'''[[Q03.0]]''' Malformations of aqueduct of Sylvius
  
''Excludes1''
+
Anomaly of aqueduct of Sylvius
  
Cesarean delivery for present delivery (P03.4)
+
Obstruction of aqueduct of Sylvius, congenital
  
damage to placenta from amniocentesis, Cesarean delivery or surgical induction (P02.1)
+
Stenosis of aqueduct of Sylvius
  
previous surgery to uterus or pelvic organs (P03.89)
+
*'''[[Q03.1]]''' Atresia of foramina of Magendie and Luschka
  
''Excludes2''
+
Dandy-Walker syndrome
  
newborn affected by complication of (fetal) intrauterine procedure (P96.5)
+
*'''[[Q03.8]]''' Other congenital hydrocephalus
  
*'''[[P00.7]]''' Newborn affected by other medical procedures on mother, not elsewhere classified
+
*'''[[Q03.9]]''' Congenital hydrocephalus, unspecified
  
Newborn affected by radiation to mother
+
*'''[[Q04]]''' Other congenital malformations of brain
  
 
''Excludes1''  
 
''Excludes1''  
  
damage to placenta from amniocentesis, cesarean delivery or surgical induction (P02.1)  
+
cyclopia (Q87.0)  
  
newborn affected by other complications of labor and delivery (P03.-)
+
macrocephaly (Q75.3)
  
*'''[[P00.8]]''' Newborn affected by other maternal conditions
+
*'''[[Q04.0]]''' Congenital malformations of corpus callosum
  
*'''[[P00.81]]''' Newborn affected by periodontal disease in mother
+
Agenesis of corpus callosum
  
*'''[[P00.89]]''' Newborn affected by other maternal conditions
+
*'''[[Q04.1]]''' Arhinencephaly
  
Newborn affected by conditions classifiable to T80-T88
+
*'''[[Q04.2]]''' Holoprosencephaly
  
Newborn affected by maternal genital tract or other localized infections
+
*'''[[Q04.3]]''' Other reduction deformities of brain
  
Newborn affected by maternal systemic lupus erythematosus
+
Absence of part of brain
  
*'''[[P00.9]]''' Newborn affected by unspecified maternal condition
+
Agenesis of part of brain
  
*'''[[P01]]''' Newborn affected by maternal complications of pregnancy ''Code first''
+
Agyria
  
any current condition in newborn
+
Aplasia of part of brain
  
''Excludes2''
+
Hydranencephaly
  
encounter for observation of newborn for suspected diseases and conditions ruled out (Z05.-)
+
Hypoplasia of part of brain
  
*'''[[P01.0]]''' Newborn affected by incompetent cervix
+
Lissencephaly
  
*'''[[P01.1]]''' Newborn affected by premature rupture of membranes
+
Microgyria
  
*'''[[P01.2]]''' Newborn affected by oligohydramnios
+
Pachygyria
  
 
''Excludes1''  
 
''Excludes1''  
  
oligohydramnios due to premature rupture of membranes (P01.1)
+
congenital malformations of corpus callosum (Q04.0)
  
*'''[[P01.3]]''' Newborn affected by polyhydramnios
+
*'''[[Q04.4]]''' Septo-optic dysplasia of brain
  
Newborn affected by hydramnios
+
*'''[[Q04.5]]''' Megalencephaly
  
*'''[[P01.4]]''' Newborn affected by ectopic pregnancy
+
*'''[[Q04.6]]''' Congenital cerebral cysts
  
Newborn affected by abdominal pregnancy
+
Porencephaly
  
*'''[[P01.5]]''' Newborn affected by multiple pregnancy
+
Schizencephaly
  
Newborn affected by triplet (pregnancy)
+
''Excludes1''
  
Newborn affected by twin (pregnancy)
+
acquired porencephalic cyst (G93.0)
  
*'''[[P01.6]]''' Newborn affected by maternal death
+
*'''[[Q04.8]]''' Other specified congenital malformations of brain
  
*'''[[P01.7]]''' Newborn affected by malpresentation before labor
+
Arnold-Chiari syndrome, type IV
  
Newborn affected by breech presentation before labor
+
Macrogyria
  
Newborn affected by external version before labor
+
*'''[[Q04.9]]''' Congenital malformation of brain, unspecified
  
Newborn affected by face presentation before labor
+
Congenital anomaly NOS of brain
  
Newborn affected by transverse lie before labor
+
Congenital deformity NOS of brain
  
Newborn affected by unstable lie before labor
+
Congenital disease or lesion NOS of brain
  
*'''[[P01.8]]''' Newborn affected by other maternal complications of pregnancy
+
Multiple anomalies NOS of brain, congenital
  
*'''[[P01.9]]''' Newborn affected by maternal complication of pregnancy, unspecified
+
*'''[[Q05]]''' Spina bifida
 +
 
 +
''Includes''
  
*'''[[P02]]''' Newborn affected by complications of placenta, cord and membranes ''Code first''
+
hydromeningocele (spinal)
  
any current condition in newborn
+
meningocele (spinal)
  
''Excludes2''
+
meningomyelocele
  
encounter for observation of newborn for suspected diseases and conditions ruled out (Z05.-)
+
myelocele
  
*'''[[P02.0]]''' Newborn affected by placenta previa
+
myelomeningocele
  
*'''[[P02.1]]''' Newborn affected by other forms of placental separation and hemorrhage
+
rachischisis
  
Newborn affected by abruptio placenta
+
spina bifida (aperta)(cystica)
  
Newborn affected by accidental hemorrhage
+
syringomyelocele ''Use additional'' code for any associated
  
Newborn affected by antepartum hemorrhage
+
paraplegia (paraparesis) (G82.2-)
  
Newborn affected by damage to placenta from amniocentesis, cesarean delivery or surgical induction
+
''Excludes1''
  
Newborn affected by maternal blood loss
+
Arnold-Chiari syndrome, type II (Q07.0-)
  
Newborn affected by premature separation of placenta
+
spina bifida occulta (Q76.0)
  
*'''[[P02.2]]''' Newborn affected by other and unspecified morphological and functional abnormalities of placenta
+
*'''[[Q05.0]]''' Cervical spina bifida with hydrocephalus
  
*'''[[P02.20]]''' Newborn affected by unspecified morphological and functional abnormalities of placenta
+
*'''[[Q05.1]]''' Thoracic spina bifida with hydrocephalus
  
*'''[[P02.29]]''' Newborn affected by other morphological and functional abnormalities of placenta
+
Dorsal spina bifida with hydrocephalus
  
Newborn affected by placental dysfunction
+
Thoracolumbar spina bifida with hydrocephalus
  
Newborn affected by placental infarction
+
*'''[[Q05.2]]''' Lumbar spina bifida with hydrocephalus
  
Newborn affected by placental insufficiency
+
Lumbosacral spina bifida with hydrocephalus
  
*'''[[P02.3]]''' Newborn affected by placental transfusion syndromes
+
*'''[[Q05.3]]''' Sacral spina bifida with hydrocephalus
  
Newborn affected by placental and cord abnormalities resulting in twin-to-twin or other transplacental
+
*'''[[Q05.4]]''' Unspecified spina bifida with hydrocephalus
  
transfusion
+
*'''[[Q05.5]]''' Cervical spina bifida without hydrocephalus
  
*'''[[P02.4]]''' Newborn affected by prolapsed cord
+
*'''[[Q05.6]]''' Thoracic spina bifida without hydrocephalus
  
*'''[[P02.5]]''' Newborn affected by other compression of umbilical cord
+
Dorsal spina bifida NOS
  
Newborn affected by umbilical cord (tightly) around neck
+
Thoracolumbar spina bifida NOS
  
Newborn affected by entanglement of umbilical cord
+
*'''[[Q05.7]]''' Lumbar spina bifida without hydrocephalus
  
Newborn affected by knot in umbilical cord
+
Lumbosacral spina bifida NOS
  
*'''[[P02.6]]''' Newborn affected by other and unspecified conditions of umbilical cord
+
*'''[[Q05.8]]''' Sacral spina bifida without hydrocephalus
  
*'''[[P02.60]]''' Newborn affected by unspecified conditions of umbilical cord
+
*'''[[Q05.9]]''' Spina bifida, unspecified
  
*'''[[P02.69]]''' Newborn affected by other conditions of umbilical cord
+
*'''[[Q06]]''' Other congenital malformations of spinal cord
  
Newborn affected by short umbilical cord
+
*'''[[Q06.0]]''' Amyelia
  
Newborn affected by vasa previa
+
*'''[[Q06.1]]''' Hypoplasia and dysplasia of spinal cord
  
''Excludes1''
+
Atelomyelia
  
newborn affected by single umbilical artery (Q27.0)
+
Myelatelia
  
*'''[[P02.7]]''' Newborn affected by chorioamnionitis
+
Myelodysplasia of spinal cord
  
*'''[[P02.70]]''' Newborn affected by fetal inflammatory response syndrome
+
*'''[[Q06.2]]''' Diastematomyelia
  
Newborn affected by FIRS
+
*'''[[Q06.3]]''' Other congenital cauda equina malformations
  
*'''[[P02.78]]''' Newborn affected by other conditions from chorioamnionitis
+
*'''[[Q06.4]]''' Hydromyelia
  
Newborn affected by amnionitis
+
Hydrorachis
  
Newborn affected by membranitis
+
*'''[[Q06.8]]''' Other specified congenital malformations of spinal cord
  
Newborn affected by placentitis
+
*'''[[Q06.9]]''' Congenital malformation of spinal cord, unspecified
  
*'''[[P02.8]]''' Newborn affected by other abnormalities of membranes
+
Congenital anomaly NOS of spinal cord
  
*'''[[P02.9]]''' Newborn affected by abnormality of membranes, unspecified
+
Congenital deformity NOS of spinal cord
  
*'''[[P03]]''' Newborn affected by other complications of labor and delivery ''Code first''
+
Congenital disease or lesion NOS of spinal cord
  
any current condition in newborn
+
*'''[[Q07]]''' Other congenital malformations of nervous system
  
 
''Excludes2''  
 
''Excludes2''  
  
encounter for observation of newborn for suspected diseases and conditions ruled out (Z05.-)
+
congenital central alveolar hypoventilation syndrome (G47.35)  
  
*'''[[P03.0]]''' Newborn affected by breech delivery and extraction
+
familial dysautonomia (Riley-Day) (G90.1)
  
*'''[[P03.1]]''' Newborn affected by other malpresentation, malposition and disproportion during labor and delivery
+
neurofibromatosis (nonmalignant) (Q85.0-)
  
Newborn affected by contracted pelvis
+
*'''[[Q07.0]]''' Arnold-Chiari syndrome
  
Newborn affected by conditions classifiable to O64-O66
+
Arnold-Chiari syndrome, type II
  
Newborn affected by persistent occipitoposterior
+
''Excludes1''
  
Newborn affected by transverse lie
+
Arnold-Chiari syndrome, type III (Q01.-)
  
*'''[[P03.2]]''' Newborn affected by forceps delivery
+
Arnold-Chiari syndrome, type IV (Q04.8)
  
*'''[[P03.3]]''' Newborn affected by delivery by vacuum extractor (ventouse)
+
*'''[[Q07.00]]''' Arnold-Chiari syndrome without spina bifida or hydrocephalus
  
*'''[[P03.4]]''' Newborn affected by Cesarean delivery
+
*'''[[Q07.01]]''' Arnold-Chiari syndrome with spina bifida
  
*'''[[P03.5]]''' Newborn affected by precipitate delivery
+
*'''[[Q07.02]]''' Arnold-Chiari syndrome with hydrocephalus
  
Newborn affected by rapid second stage
+
*'''[[Q07.03]]''' Arnold-Chiari syndrome with spina bifida and hydrocephalus
  
*'''[[P03.6]]''' Newborn affected by abnormal uterine contractions
+
*'''[[Q07.8]]''' Other specified congenital malformations of nervous system
  
Newborn affected by conditions classifiable to O62.-, except O62.3
+
Agenesis of nerve
  
Newborn affected by hypertonic labor
+
Displacement of brachial plexus
  
Newborn affected by uterine inertia
+
Jaw-winking syndrome
  
*'''[[P03.8]]''' Newborn affected by other specified complications of labor and delivery
+
Marcus Gunn's syndrome
  
*'''[[P03.81]]''' Newborn affected by abnormality in fetal (intrauterine) heart rate or rhythm
+
*'''[[Q07.9]]''' Congenital malformation of nervous system, unspecified
  
''Excludes1''
+
Congenital anomaly NOS of nervous system
  
neonatal cardiac dysrhythmia (P29.1-)
+
Congenital deformity NOS of nervous system
  
*'''[[P03.810]]''' Newborn affected by abnormality in fetal (intrauterine) heart rate or rhythm before the
+
Congenital disease or lesion NOS of nervous system
  
onset of labor
+
Congenital malformations of eye, ear, face and neck (Q10-Q18)
  
*'''[[P03.811]]''' Newborn affected by abnormality in fetal (intrauterine) heart rate or rhythm during labor
+
''Excludes2''  
  
*'''[[P03.819]]''' Newborn affected by abnormality in fetal (intrauterine) heart rate or rhythm, unspecified
+
cleft lip and cleft palate (Q35-Q37)  
  
as to time of onset
+
congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
  
*'''[[P03.82]]''' Meconium passage during delivery
+
congenital malformation of larynx (Q31.-)
  
''Excludes1''
+
congenital malformation of lip NEC (Q38.0)
  
meconium aspiration (P24.00, P24.01)  
+
congenital malformation of nose (Q30.-)  
  
meconium staining (P96.83)
+
congenital malformation of parathyroid gland (Q89.2)  
  
*'''[[P03.89]]''' Newborn affected by other specified complications of labor and delivery
+
congenital malformation of thyroid gland (Q89.2)
  
Newborn affected by abnormality of maternal soft tissues
+
*'''[[Q10]]''' Congenital malformations of eyelid, lacrimal apparatus and orbit
  
Newborn affected by conditions classifiable to O60-O75 and by procedures used in labor and delivery
+
''Excludes1''
  
not included in P02.- and P03.0-P03.6
+
cryptophthalmos NOS (Q11.2)
  
Newborn affected by induction of labor
+
cryptophthalmos syndrome (Q87.0)
  
*'''[[P03.9]]''' Newborn affected by complication of labor and delivery, unspecified
+
*'''[[Q10.0]]''' Congenital ptosis
  
*'''[[P04]]''' Newborn affected by noxious substances transmitted via placenta or breast milk
+
*'''[[Q10.1]]''' Congenital ectropion
  
''Includes''  
+
*'''[[Q10.2]]''' Congenital entropion
  
nonteratogenic effects of substances transmitted via placenta
+
*'''[[Q10.3]]''' Other congenital malformations of eyelid
  
''Excludes2''
+
Ablepharon
  
congenital malformations (Q00-Q99)
+
Blepharophimosis, congenital  
  
encounter for observation of newborn for suspected diseases and conditions ruled out (Z05.-)
+
Coloboma of eyelid
  
neonatal jaundice from excessive hemolysis due to drugs or toxins transmitted from mother (P58.4)
+
Congenital absence or agenesis of cilia
  
newborn in contact with and (suspected) exposures hazardous to health not transmitted via placenta or  
+
Congenital absence or agenesis of eyelid
  
breast milk (Z77.-)
+
Congenital accessory eyelid
  
*'''[[P04.0]]''' Newborn affected by maternal anesthesia and analgesia in pregnancy, labor and delivery
+
Congenital accessory eye muscle
  
Newborn affected by reactions and intoxications from maternal opiates and tranquilizers administered for
+
Congenital malformation of eyelid NOS
  
procedures during pregnancy or labor and delivery
+
*'''[[Q10.4]]''' Absence and agenesis of lacrimal apparatus
  
''Excludes2''
+
Congenital absence of punctum lacrimale
  
newborn affected by other maternal medication (P04.1-)
+
*'''[[Q10.5]]''' Congenital stenosis and stricture of lacrimal duct
  
*'''[[P04.1]]''' Newborn affected by other maternal medication ''Code first''
+
*'''[[Q10.6]]''' Other congenital malformations of lacrimal apparatus
  
withdrawal symptoms from maternal use of drugs of addiction, if applicable (P96.1)
+
Congenital malformation of lacrimal apparatus NOS
  
''Excludes1''  
+
*'''[[Q10.7]]''' Congenital malformation of orbit
  
dysmorphism due to warfarin (Q86.2)
+
*'''[[Q11]]''' Anophthalmos, microphthalmos and macrophthalmos
  
fetal hydantoin syndrome (Q86.1)
+
*'''[[Q11.0]]''' Cystic eyeball
  
''Excludes2''  
+
*'''[[Q11.1]]''' Other anophthalmos
  
maternal anesthesia and analgesia in pregnancy, labor and delivery (P04.0)
+
Anophthalmos NOS
  
maternal use of drugs of addiction (P04.4-)
+
Agenesis of eye
  
*'''[[P04.11]]''' Newborn affected by maternal antineoplastic chemotherapy
+
Aplasia of eye
  
*'''[[P04.12]]''' Newborn affected by maternal cytotoxic drugs
+
*'''[[Q11.2]]''' Microphthalmos
  
*'''[[P04.13]]''' Newborn affected by maternal use of anticonvulsants
+
Cryptophthalmos NOS
  
*'''[[P04.14]]''' Newborn affected by maternal use of opiates
+
Dysplasia of eye
  
*'''[[P04.15]]''' Newborn affected by maternal use of antidepressants
+
Hypoplasia of eye
  
*'''[[P04.16]]''' Newborn affected by maternal use of amphetamines
+
Rudimentary eye
  
*'''[[P04.17]]''' Newborn affected by maternal use of sedative-hypnotics
+
''Excludes1''  
  
*'''[[P04.1A]] Newborn affected by maternal use of anxiolytics'''
+
cryptophthalmos syndrome (Q87.0)
  
*'''[[P04.18]]''' Newborn affected by other maternal medication
+
*'''[[Q11.3]]''' Macrophthalmos
  
*'''[[P04.19]]''' Newborn affected by maternal use of unspecified medication
+
''Excludes1''  
  
*'''[[P04.2]]''' Newborn affected by maternal use of tobacco
+
macrophthalmos in congenital glaucoma (Q15.0)
  
Newborn affected by exposure in utero to tobacco smoke
+
*'''[[Q12]]''' Congenital lens malformations
  
''Excludes2''  
+
*'''[[Q12.0]]''' Congenital cataract
  
newborn exposure to environmental tobacco smoke (P96.81)
+
*'''[[Q12.1]]''' Congenital displaced lens
  
*'''[[P04.3]]''' Newborn affected by maternal use of alcohol
+
*'''[[Q12.2]]''' Coloboma of lens
  
''Excludes1''  
+
*'''[[Q12.3]]''' Congenital aphakia
  
fetal alcohol syndrome (Q86.0)
+
*'''[[Q12.4]]''' Spherophakia
  
*'''[[P04.4]]''' Newborn affected by maternal use of drugs of addiction
+
*'''[[Q12.8]]''' Other congenital lens malformations
  
*'''[[P04.40]]''' Newborn affected by maternal use of unspecified drugs of addiction
+
Microphakia
  
*'''[[P04.41]]''' Newborn affected by maternal use of cocaine
+
*'''[[Q12.9]]''' Congenital lens malformation, unspecified
  
*'''[[P04.42]]''' Newborn affected by maternal use of hallucinogens
+
*'''[[Q13]]''' Congenital malformations of anterior segment of eye
  
''Excludes2''  
+
*'''[[Q13.0]]''' Coloboma of iris
  
newborn affected by other maternal medication (P04.1-)
+
Coloboma NOS
  
*'''[[P04.49]]''' Newborn affected by maternal use of other drugs of addiction
+
*'''[[Q13.1]]''' Absence of iris
  
''Excludes2''  
+
Aniridia ''Use additional''  
  
newborn affected by maternal anesthesia and analgesia (P04.0)  
+
code for associated glaucoma (H42)
  
withdrawal symptoms from maternal use of drugs of addiction (P96.1)
+
*'''[[Q13.2]]''' Other congenital malformations of iris
  
*'''[[P04.5]]''' Newborn affected by maternal use of nutritional chemical substances
+
Anisocoria, congenital
  
*'''[[P04.6]]''' Newborn affected by maternal exposure to environmental chemical substances
+
Atresia of pupil
  
*'''[[P04.8]]''' Newborn affected by other maternal noxious substances
+
Congenital malformation of iris NOS
  
*'''[[P04.81]]''' Newborn affected by maternal use of cannabis
+
Corectopia
  
*'''[[P04.89]]''' Newborn affected by other maternal noxious substances
+
*'''[[Q13.3]]''' Congenital corneal opacity
  
*'''[[P04.9]]''' Newborn affected by maternal noxious substance, unspecified
+
*'''[[Q13.4]]''' Other congenital corneal malformations
  
Disorders of newborn related to length of gestation and fetal growth (P05-P08)
+
Congenital malformation of cornea NOS
  
*'''[[P05]]''' Disorders of newborn related to slow fetal growth and fetal malnutrition
+
Microcornea
  
*'''[[P05.0]]''' Newborn light for gestational age
+
Peter's anomaly
  
Newborn light-for-dates
+
*'''[[Q13.5]]''' Blue sclera
  
Weight below but length above 10th percentile for gestational age
+
*'''[[Q13.8]]''' Other congenital malformations of anterior segment of eye
  
*'''[[P05.00]]''' Newborn light for gestational age, unspecified weight
+
*'''[[Q13.81]]''' Rieger's anomaly ''Use additional''
  
*'''[[P05.01]]''' Newborn light for gestational age, less than 500 grams
+
code for associated glaucoma (H42)
  
*'''[[P05.02]]''' Newborn light for gestational age, 500-749 grams
+
*'''[[Q13.89]]''' Other congenital malformations of anterior segment of eye
  
*'''[[P05.03]]''' Newborn light for gestational age, 750-999 grams
+
*'''[[Q13.9]]''' Congenital malformation of anterior segment of eye, unspecified
  
*'''[[P05.04]]''' Newborn light for gestational age, 1000-1249 grams
+
*'''[[Q14]]''' Congenital malformations of posterior segment of eye
  
*'''[[P05.05]]''' Newborn light for gestational age, 1250-1499 grams
+
''Excludes2''  
  
*'''[[P05.06]]''' Newborn light for gestational age, 1500-1749 grams
+
optic nerve hypoplasia (H47.03-)
  
*'''[[P05.07]]''' Newborn light for gestational age, 1750-1999 grams
+
*'''[[Q14.0]]''' Congenital malformation of vitreous humor
  
*'''[[P05.08]]''' Newborn light for gestational age, 2000-2499 grams
+
Congenital vitreous opacity
  
*'''[[P05.09]]''' Newborn light for gestational age, 2500 grams and over
+
*'''[[Q14.1]]''' Congenital malformation of retina
  
Newborn light for gestational age, other
+
Congenital retinal aneurysm
  
*'''[[P05.1]]''' Newborn small for gestational age
+
*'''[[Q14.2]]''' Congenital malformation of optic disc
  
Newborn small-and-light-for-dates
+
Coloboma of optic disc
  
Newborn small-for-dates
+
*'''[[Q14.3]]''' Congenital malformation of choroid
  
Weight and length below 10th percentile for gestational age
+
*'''[[Q14.8]]''' Other congenital malformations of posterior segment of eye
  
*'''[[P05.10]]''' Newborn small for gestational age, unspecified weight
+
Coloboma of the fundus
  
*'''[[P05.11]]''' Newborn small for gestational age, less than 500 grams
+
*'''[[Q14.9]]''' Congenital malformation of posterior segment of eye, unspecified
  
*'''[[P05.12]]''' Newborn small for gestational age, 500-749 grams
+
*'''[[Q15]]''' Other congenital malformations of eye
  
*'''[[P05.13]]''' Newborn small for gestational age, 750-999 grams
+
''Excludes1''  
  
*'''[[P05.14]]''' Newborn small for gestational age, 1000-1249 grams
+
congenital nystagmus (H55.01)
  
*'''[[P05.15]]''' Newborn small for gestational age, 1250-1499 grams
+
ocular albinism (E70.31-)
  
*'''[[P05.16]]''' Newborn small for gestational age, 1500-1749 grams
+
optic nerve hypoplasia (H47.03-)
  
*'''[[P05.17]]''' Newborn small for gestational age, 1750-1999 grams
+
retinitis pigmentosa (H35.52)
  
*'''[[P05.18]]''' Newborn small for gestational age, 2000-2499 grams
+
*'''[[Q15.0]]''' Congenital glaucoma
  
*'''[[P05.19]]''' Newborn small for gestational age, other
+
Axenfeld's anomaly
  
Newborn small for gestational age, 2500 grams and over
+
Buphthalmos
  
*'''[[P05.2]]''' Newborn affected by fetal (intrauterine) malnutrition not light or small for gestational age
+
Glaucoma of childhood
  
Infant, not light or small for gestational age, showing signs of fetal malnutrition, such as dry, peeling skin and
+
Glaucoma of newborn
  
loss of subcutaneous tissue
+
Hydrophthalmos
  
''Excludes1''
+
Keratoglobus, congenital, with glaucoma
  
newborn affected by fetal malnutrition with light for gestational age (P05.0-)
+
Macrocornea with glaucoma
  
newborn affected by fetal malnutrition with small for gestational age (P05.1-)
+
Macrophthalmos in congenital glaucoma
  
*'''[[P05.9]]''' Newborn affected by slow intrauterine growth, unspecified
+
Megalocornea with glaucoma
  
Newborn affected by fetal growth retardation NOS
+
*'''[[Q15.8]]''' Other specified congenital malformations of eye
  
*'''[[P07]]''' Disorders of newborn related to short gestation and low birth weight, not elsewhere classified
+
*'''[[Q15.9]]''' Congenital malformation of eye, unspecified
  
Note
+
Congenital anomaly of eye
  
When both birth weight and gestational age of the newborn are available, both should be coded with birth
+
Congenital deformity of eye
  
weight sequenced before gestational age
+
*'''[[Q16]]''' Congenital malformations of ear causing impairment of hearing
  
''Includes''  
+
''Excludes1''  
  
the listed conditions, without further specification, as the cause of morbidity or additional care, in newborn
+
congenital deafness (H90.-)
  
*'''[[P07.0]]''' Extremely low birth weight newborn
+
*'''[[Q16.0]]''' Congenital absence of (ear) auricle
  
Newborn birth weight 999 g. or less
+
*'''[[Q16.1]]''' Congenital absence, atresia and stricture of auditory canal (external)
  
''Excludes1''
+
Congenital atresia or stricture of osseous meatus
  
low birth weight due to slow fetal growth and fetal malnutrition (P05.-)
+
*'''[[Q16.2]]''' Absence of eustachian tube
  
*'''[[P07.00]]''' Extremely low birth weight newborn, unspecified weight
+
*'''[[Q16.3]]''' Congenital malformation of ear ossicles
  
*'''[[P07.01]]''' Extremely low birth weight newborn, less than 500 grams
+
Congenital fusion of ear ossicles
  
*'''[[P07.02]]''' Extremely low birth weight newborn, 500-749 grams
+
*'''[[Q16.4]]''' Other congenital malformations of middle ear
  
*'''[[P07.03]]''' Extremely low birth weight newborn, 750-999 grams
+
Congenital malformation of middle ear NOS
  
*'''[[P07.1]]''' Other low birth weight newborn
+
*'''[[Q16.5]]''' Congenital malformation of inner ear
  
Newborn birth weight 1000-2499 g
+
Congenital anomaly of membranous labyrinth
  
''Excludes1''
+
Congenital anomaly of organ of Corti
  
low birth weight due to slow fetal growth and fetal malnutrition (P05.-)
+
*'''[[Q16.9]]''' Congenital malformation of ear causing impairment of hearing, unspecified
  
*'''[[P07.10]]''' Other low birth weight newborn, unspecified weight
+
Congenital absence of ear NOS
  
*'''[[P07.14]]''' Other low birth weight newborn, 1000-1249 grams
+
*'''[[Q17]]''' Other congenital malformations of ear
  
*'''[[P07.15]]''' Other low birth weight newborn, 1250-1499 grams
+
''Excludes1''  
  
*'''[[P07.16]]''' Other low birth weight newborn, 1500-1749 grams
+
congenital malformations of ear with impairment of hearing (Q16.0-Q16.9)
  
*'''[[P07.17]]''' Other low birth weight newborn, 1750-1999 grams
+
preauricular sinus (Q18.1)
  
*'''[[P07.18]]''' Other low birth weight newborn, 2000-2499 grams
+
*'''[[Q17.0]]''' Accessory auricle
  
*'''[[P07.2]]''' Extreme immaturity of newborn
+
Accessory tragus
  
Less than 28 completed weeks (less than 196 completed days) of gestation
+
Polyotia
  
*'''[[P07.20]]''' Extreme immaturity of newborn, unspecified weeks of gestation
+
Preauricular appendage or tag
  
Gestational age less than 28 completed weeks NOS
+
Supernumerary ear
  
*'''[[P07.21]]''' Extreme immaturity of newborn, gestational age less than 23 completed weeks
+
Supernumerary lobule
  
Extreme immaturity of newborn, gestational age less than 23 weeks, 0 days
+
*'''[[Q17.1]]''' Macrotia
  
*'''[[P07.22]]''' Extreme immaturity of newborn, gestational age 23 completed weeks
+
*'''[[Q17.2]]''' Microtia
  
Extreme immaturity of newborn, gestational age 23 weeks, 0 days through 23 weeks, 6 days
+
*'''[[Q17.3]]''' Other misshapen ear
  
*'''[[P07.23]]''' Extreme immaturity of newborn, gestational age 24 completed weeks
+
Pointed ear
  
Extreme immaturity of newborn, gestational age 24 weeks, 0 days through 24 weeks, 6 days
+
*'''[[Q17.4]]''' Misplaced ear
  
*'''[[P07.24]]''' Extreme immaturity of newborn, gestational age 25 completed weeks
+
Low-set ears
  
Extreme immaturity of newborn, gestational age 25 weeks, 0 days through 25 weeks, 6 days
+
''Excludes1''
  
*'''[[P07.25]]''' Extreme immaturity of newborn, gestational age 26 completed weeks
+
cervical auricle (Q18.2)
  
Extreme immaturity of newborn, gestational age 26 weeks, 0 days through 26 weeks, 6 days
+
*'''[[Q17.5]]''' Prominent ear
  
*'''[[P07.26]]''' Extreme immaturity of newborn, gestational age 27 completed weeks
+
Bat ear
  
Extreme immaturity of newborn, gestational age 27 weeks, 0 days through 27 weeks, 6 days
+
*'''[[Q17.8]]''' Other specified congenital malformations of ear
  
*'''[[P07.3]]''' Preterm (premature) newborn (other)
+
Congenital absence of lobe of ear
  
28 completed weeks or more but less than 37 completed weeks (196 completed days but less than 259
+
*'''[[Q17.9]]''' Congenital malformation of ear, unspecified
  
completed days) of gestation
+
Congenital anomaly of ear NOS
  
'''Prematurity NOS'''
+
*'''[[Q18]]''' Other congenital malformations of face and neck
  
*'''[[P07.30]]''' Preterm newborn, unspecified weeks of gestation
+
''Excludes1''  
 
 
*'''[[P07.31]]''' Preterm newborn, gestational age 28 completed weeks
 
  
Preterm newborn, gestational age 28 weeks, 0 days through 28 weeks, 6 days
+
cleft lip and cleft palate (Q35-Q37)
  
*'''[[P07.32]]''' Preterm newborn, gestational age 29 completed weeks
+
conditions classified to Q67.0-Q67.4
  
Preterm newborn, gestational age 29 weeks, 0 days through 29 weeks, 6 days
+
congenital malformations of skull and face bones (Q75.-)
  
*'''[[P07.33]]''' Preterm newborn, gestational age 30 completed weeks
+
cyclopia (Q87.0)
  
Preterm newborn, gestational age 30 weeks, 0 days through 30 weeks, 6 days
+
dentofacial anomalies (including malocclusion) (M26.-)
  
*'''[[P07.34]]''' Preterm newborn, gestational age 31 completed weeks
+
malformation syndromes affecting facial appearance (Q87.0)
  
Preterm newborn, gestational age 31 weeks, 0 days through 31 weeks, 6 days
+
persistent thyroglossal duct (Q89.2)
  
*'''[[P07.35]]''' Preterm newborn, gestational age 32 completed weeks
+
*'''[[Q18.0]]''' Sinus, fistula and cyst of branchial cleft
  
Preterm newborn, gestational age 32 weeks, 0 days through 32 weeks, 6 days
+
Branchial vestige
  
*'''[[P07.36]]''' Preterm newborn, gestational age 33 completed weeks
+
*'''[[Q18.1]]''' Preauricular sinus and cyst
  
Preterm newborn, gestational age 33 weeks, 0 days through 33 weeks, 6 days
+
Fistula of auricle, congenital
  
*'''[[P07.37]]''' Preterm newborn, gestational age 34 completed weeks
+
Cervicoaural fistula
  
Preterm newborn, gestational age 34 weeks, 0 days through 34 weeks, 6 days
+
*'''[[Q18.2]]''' Other branchial cleft malformations
  
*'''[[P07.38]]''' Preterm newborn, gestational age 35 completed weeks
+
Branchial cleft malformation NOS
  
Preterm newborn, gestational age 35 weeks, 0 days through 35 weeks, 6 days
+
Cervical auricle
  
*'''[[P07.39]]''' Preterm newborn, gestational age 36 completed weeks
+
Otocephaly
  
Preterm newborn, gestational age 36 weeks, 0 days through 36 weeks, 6 days
+
*'''[[Q18.3]]''' Webbing of neck
  
*'''[[P08]]''' Disorders of newborn related to long gestation and high birth weight
+
Pterygium colli
  
Note
+
*'''[[Q18.4]]''' Macrostomia
  
When both birth weight and gestational age of the newborn are available, priority of assignment should be
+
*'''[[Q18.5]]''' Microstomia
  
given to birth weight
+
*'''[[Q18.6]]''' Macrocheilia
  
''Includes''
+
Hypertrophy of lip, congenital
  
the listed conditions, without further specification, as causes of morbidity or additional care, in newborn
+
*'''[[Q18.7]]''' Microcheilia
  
*'''[[P08.0]]''' Exceptionally large newborn baby
+
*'''[[Q18.8]]''' Other specified congenital malformations of face and neck
  
Usually implies a birth weight of 4500 g. or more
+
Medial cyst of face and neck
  
''Excludes1''
+
Medial fistula of face and neck
  
syndrome of infant of diabetic mother (P70.1)
+
Medial sinus of face and neck
  
syndrome of infant of mother with gestational diabetes (P70.0)
+
*'''[[Q18.9]]''' Congenital malformation of face and neck, unspecified
  
*'''[[P08.1]]''' Other heavy for gestational age newborn
+
Congenital anomaly NOS of face and neck
  
Other newborn heavy- or large-for-dates regardless of period of gestation
+
Congenital malformations of the circulatory system (Q20-Q28)
  
Usually implies a birth weight of 4000 g. to 4499 g
+
*'''[[Q20]]''' Congenital malformations of cardiac chambers and connections
  
 
''Excludes1''  
 
''Excludes1''  
  
newborn with a birth weight of 4500 or more (P08.0)  
+
dextrocardia with situs inversus (Q89.3)  
  
syndrome of infant of diabetic mother (P70.1)  
+
mirror-image atrial arrangement with situs inversus (Q89.3)
  
syndrome of infant of mother with gestational diabetes (P70.0)
+
*'''[[Q20.0]]''' Common arterial trunk
  
*'''[[P08.2]]''' Late newborn, not heavy for gestational age
+
Persistent truncus arteriosus
  
*'''[[P08.21]]''' Post-term newborn
+
''Excludes1''  
  
Newborn with gestation period over 40 completed weeks to 42 completed weeks
+
aortic septal defect (Q21.4)
  
*'''[[P08.22]]''' Prolonged gestation of newborn
+
*'''[[Q20.1]]''' Double outlet right ventricle
  
Newborn with gestation period over 42 completed weeks (294 days or more), not heavy- or large-for-  
+
Taussig-Bing syndrome
  
dates
+
*'''[[Q20.2]]''' Double outlet left ventricle
  
'''Postmaturity NOS '''
+
*'''[[Q20.3]]''' Discordant ventriculoarterial connection
  
Abnormal findings on neonatal screening (P09)
+
Dextrotransposition of aorta
  
*'''[[P09]]''' Abnormal findings on neonatal screening ''Use additional''
+
Transposition of great vessels (complete)
  
code to identify signs, symptoms and conditions associated with the screening
+
*'''[[Q20.4]]''' Double inlet ventricle
  
''Excludes2''
+
Common ventricle
  
nonspecific serologic evidence of human immunodeficiency virus (HIV) (R75)
+
Cor triloculare biatriatum
  
Birth trauma (P10-P15)
+
Single ventricle
  
*'''[[P10]]''' Intracranial laceration and hemorrhage due to birth injury
+
*'''[[Q20.5]]''' Discordant atrioventricular connection
  
''Excludes1''
+
Corrected transposition
  
intracranial hemorrhage of newborn NOS (P52.9)
+
Levotransposition
  
intracranial hemorrhage of newborn due to anoxia or hypoxia (P52.-)
+
Ventricular inversion
  
nontraumatic intracranial hemorrhage of newborn (P52.-)
+
*'''[[Q20.6]]''' Isomerism of atrial appendages
  
*'''[[P10.0]]''' Subdural hemorrhage due to birth injury
+
Isomerism of atrial appendages with asplenia or polysplenia
  
Subdural hematoma (localized) due to birth injury
+
*'''[[Q20.8]]''' Other congenital malformations of cardiac chambers and connections
  
''Excludes1''  
+
Cor binoculare
 +
 
 +
*'''[[Q20.9]]''' Congenital malformation of cardiac chambers and connections, unspecified
  
subdural hemorrhage accompanying tentorial tear (P10.4)
+
*'''[[Q21]]''' Congenital malformations of cardiac septa
  
*'''[[P10.1]]''' Cerebral hemorrhage due to birth injury
+
''Excludes1''  
  
*'''[[P10.2]]''' Intraventricular hemorrhage due to birth injury
+
acquired cardiac septal defect (I51.0)
  
*'''[[P10.3]]''' Subarachnoid hemorrhage due to birth injury
+
*'''[[Q21.0]]''' Ventricular septal defect
  
*'''[[P10.4]]''' Tentorial tear due to birth injury
+
Roger's disease
  
*'''[[P10.8]]''' Other intracranial lacerations and hemorrhages due to birth injury
+
*'''[[Q21.1]]''' Atrial septal defect
  
*'''[[P10.9]]''' Unspecified intracranial laceration and hemorrhage due to birth injury
+
Coronary sinus defect
  
*'''[[P11]]''' Other birth injuries to central nervous system
+
Patent or persistent foramen ovale
  
*'''[[P11.0]]''' Cerebral edema due to birth injury
+
Patent or persistent ostium secundum defect (type II)
  
*'''[[P11.1]]''' Other specified brain damage due to birth injury
+
Patent or persistent sinus venosus defect
  
*'''[[P11.2]]''' Unspecified brain damage due to birth injury
+
*'''[[Q21.2]]''' Atrioventricular septal defect
  
*'''[[P11.3]]''' Birth injury to facial nerve
+
Common atrioventricular canal
  
Facial palsy due to birth injury
+
Endocardial cushion defect
  
*'''[[P11.4]]''' Birth injury to other cranial nerves
+
Ostium primum atrial septal defect (type I)
  
*'''[[P11.5]]''' Birth injury to spine and spinal cord
+
*'''[[Q21.3]]''' Tetralogy of Fallot
  
Fracture of spine due to birth injury
+
Ventricular septal defect with pulmonary stenosis or atresia, dextroposition of aorta and hypertrophy of right
  
*'''[[P11.9]]''' Birth injury to central nervous system, unspecified
+
ventricle
  
*'''[[P12]]''' Birth injury to scalp
+
*'''[[Q21.4]]''' Aortopulmonary septal defect
  
*'''[[P12.0]]''' Cephalhematoma due to birth injury
+
Aortic septal defect
  
*'''[[P12.1]]''' Chignon (from vacuum extraction) due to birth injury
+
Aortopulmonary window
  
*'''[[P12.2]]''' Epicranial subaponeurotic hemorrhage due to birth injury
+
*'''[[Q21.8]]''' Other congenital malformations of cardiac septa
  
Subgaleal hemorrhage
+
Eisenmenger's defect
  
*'''[[P12.3]]''' Bruising of scalp due to birth injury
+
Pentalogy of Fallot ''Code also''  
  
*'''[[P12.4]]''' Injury of scalp of newborn due to monitoring equipment
+
if applicable
  
Sampling incision of scalp of newborn
+
Eisenmenger's complex (I27.83)
  
Scalp clip (electrode) injury of newborn
+
Eisenmenger's syndrome (I27.83)
  
*'''[[P12.8]]''' Other birth injuries to scalp
+
*'''[[Q21.9]]''' Congenital malformation of cardiac septum, unspecified
  
*'''[[P12.81]]''' Caput succedaneum
+
Septal (heart) defect NOS
  
*'''[[P12.89]]''' Other birth injuries to scalp
+
*'''[[Q22]]''' Congenital malformations of pulmonary and tricuspid valves
  
*'''[[P12.9]]''' Birth injury to scalp, unspecified
+
*'''[[Q22.0]]''' Pulmonary valve atresia
  
*'''[[P13]]''' Birth injury to skeleton
+
*'''[[Q22.1]]''' Congenital pulmonary valve stenosis
  
''Excludes2''  
+
*'''[[Q22.2]]''' Congenital pulmonary valve insufficiency
  
birth injury to spine (P11.5)
+
Congenital pulmonary valve regurgitation
  
*'''[[P13.0]]''' Fracture of skull due to birth injury
+
*'''[[Q22.3]]''' Other congenital malformations of pulmonary valve
  
*'''[[P13.1]]''' Other birth injuries to skull
+
Congenital malformation of pulmonary valve NOS
  
''Excludes1''
+
Supernumerary cusps of pulmonary valve
  
cephalhematoma (P12.0)
+
*'''[[Q22.4]]''' Congenital tricuspid stenosis
  
*'''[[P13.2]]''' Birth injury to femur
+
Congenital tricuspid atresia
  
*'''[[P13.3]]''' Birth injury to other long bones
+
*'''[[Q22.5]]''' Ebstein's anomaly
  
*'''[[P13.4]]''' Fracture of clavicle due to birth injury
+
*'''[[Q22.6]]''' Hypoplastic right heart syndrome
  
*'''[[P13.8]]''' Birth injuries to other parts of skeleton
+
*'''[[Q22.8]]''' Other congenital malformations of tricuspid valve
  
*'''[[P13.9]]''' Birth injury to skeleton, unspecified
+
*'''[[Q22.9]]''' Congenital malformation of tricuspid valve, unspecified
  
*'''[[P14]]''' Birth injury to peripheral nervous system
+
*'''[[Q23]]''' Congenital malformations of aortic and mitral valves
  
*'''[[P14.0]]''' Erb's paralysis due to birth injury
+
*'''[[Q23.0]]''' Congenital stenosis of aortic valve
  
*'''[[P14.1]]''' Klumpke's paralysis due to birth injury
+
Congenital aortic atresia
  
*'''[[P14.2]]''' Phrenic nerve paralysis due to birth injury
+
Congenital aortic stenosis NOS
  
*'''[[P14.3]]''' Other brachial plexus birth injuries
+
''Excludes1''  
  
*'''[[P14.8]]''' Birth injuries to other parts of peripheral nervous system
+
congenital stenosis of aortic valve in hypoplastic left heart syndrome (Q23.4)
  
*'''[[P14.9]]''' Birth injury to peripheral nervous system, unspecified
+
congenital subaortic stenosis (Q24.4)
  
*'''[[P15]]''' Other birth injuries
+
supravalvular aortic stenosis (congenital) (Q25.3)
  
*'''[[P15.0]]''' Birth injury to liver
+
*'''[[Q23.1]]''' Congenital insufficiency of aortic valve
  
Rupture of liver due to birth injury
+
Bicuspid aortic valve
  
*'''[[P15.1]]''' Birth injury to spleen
+
Congenital aortic insufficiency
  
Rupture of spleen due to birth injury
+
*'''[[Q23.2]]''' Congenital mitral stenosis
  
*'''[[P15.2]]''' Sternomastoid injury due to birth injury
+
Congenital mitral atresia
  
*'''[[P15.3]]''' Birth injury to eye
+
*'''[[Q23.3]]''' Congenital mitral insufficiency
  
Subconjunctival hemorrhage due to birth injury
+
*'''[[Q23.4]]''' Hypoplastic left heart syndrome
  
Traumatic glaucoma due to birth injury
+
*'''[[Q23.8]]''' Other congenital malformations of aortic and mitral valves
  
*'''[[P15.4]]''' Birth injury to face
+
*'''[[Q23.9]]''' Congenital malformation of aortic and mitral valves, unspecified
  
Facial congestion due to birth injury
+
*'''[[Q24]]''' Other congenital malformations of heart
  
*'''[[P15.5]]''' Birth injury to external genitalia
+
''Excludes1''  
  
*'''[[P15.6]]''' Subcutaneous fat necrosis due to birth injury
+
endocardial fibroelastosis (I42.4)
  
*'''[[P15.8]]''' Other specified birth injuries
+
*'''[[Q24.0]]''' Dextrocardia
  
*'''[[P15.9]]''' Birth injury, unspecified
+
''Excludes1''  
  
Respiratory and cardiovascular disorders specific to the perinatal period (P19-P29)
+
dextrocardia with situs inversus (Q89.3)  
  
*'''[[P19]]''' Metabolic acidemia in newborn
+
isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
  
''Includes''
+
mirror-image atrial arrangement with situs inversus (Q89.3)
  
metabolic acidemia in newborn
+
*'''[[Q24.1]]''' Levocardia
  
*'''[[P19.0]]''' Metabolic acidemia in newborn first noted before onset of labor
+
*'''[[Q24.2]]''' Cor triatriatum
  
*'''[[P19.1]]''' Metabolic acidemia in newborn first noted during labor
+
*'''[[Q24.3]]''' Pulmonary infundibular stenosis
  
*'''[[P19.2]]''' Metabolic acidemia noted at birth
+
Subvalvular pulmonic stenosis
  
*'''[[P19.9]]''' Metabolic acidemia, unspecified
+
*'''[[Q24.4]]''' Congenital subaortic stenosis
  
*'''[[P22]]''' Respiratory distress of newborn
+
*'''[[Q24.5]]''' Malformation of coronary vessels
  
*'''[[P22.0]]''' Respiratory distress syndrome of newborn
+
Congenital coronary (artery) aneurysm
  
Cardiorespiratory distress syndrome of newborn
+
*'''[[Q24.6]]''' Congenital heart block
  
Hyaline membrane disease
+
*'''[[Q24.8]]''' Other specified congenital malformations of heart
  
Idiopathic respiratory distress syndrome (IRDS or RDS) of newborn
+
Congenital diverticulum of left ventricle
  
'''Pulmonary hypoperfusion syndrome'''
+
Congenital malformation of myocardium
  
Respiratory distress syndrome, type I
+
Congenital malformation of pericardium
  
''Excludes2''
+
Malposition of heart
  
respiratory arrest of newborn (P28.81)
+
Uhl's disease
  
respiratory failure of newborn NOS (P28.5)
+
*'''[[Q24.9]]''' Congenital malformation of heart, unspecified
  
*'''[[P22.1]]''' Transient tachypnea of newborn
+
Congenital anomaly of heart
  
Idiopathic tachypnea of newborn
+
Congenital disease of heart
  
Respiratory distress syndrome, type II
+
*'''[[Q25]]''' Congenital malformations of great arteries
  
Wet lung syndrome
+
*'''[[Q25.0]]''' Patent ductus arteriosus
  
*'''[[P22.8]]''' Other respiratory distress of newborn
+
Patent ductus Botallo
  
''Excludes1''
+
Persistent ductus arteriosus
  
respiratory arrest of newborn (P28.81)
+
*'''[[Q25.1]]''' Coarctation of aorta
  
respiratory failure of newborn NOS (P28.5)
+
Coarctation of aorta (preductal) (postductal)
  
*'''[[P22.9]]''' Respiratory distress of newborn, unspecified
+
Stenosis of aorta
  
''Excludes1''  
+
*'''[[Q25.2]]''' Atresia of aorta
  
respiratory arrest of newborn (P28.81)
+
*'''[[Q25.21]]''' Interruption of aortic arch
  
respiratory failure of newborn NOS (P28.5)
+
Atresia of aortic arch
  
*'''[[P23]]''' Congenital pneumonia
+
*'''[[Q25.29]]''' Other atresia of aorta
  
''Includes''
+
Atresia of aorta
  
infective pneumonia acquired in utero or during birth
+
*'''[[Q25.3]]''' Supravalvular aortic stenosis
  
 
''Excludes1''  
 
''Excludes1''  
  
neonatal pneumonia resulting from aspiration (P24.-)
+
congenital aortic stenosis NOS (Q23.0)  
  
*'''[[P23.0]]''' Congenital pneumonia due to viral agent ''Use additional''
+
congenital stenosis of aortic valve (Q23.0)
  
code (B97) to identify organism
+
*'''[[Q25.4]]''' Other congenital malformations of aorta
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital rubella pneumonitis (P35.0)
+
hypoplasia of aorta in hypoplastic left heart syndrome (Q23.4)
 
 
*'''[[P23.1]]''' Congenital pneumonia due to Chlamydia
 
  
*'''[[P23.2]]''' Congenital pneumonia due to staphylococcus
+
*'''[[Q25.40]]''' Congenital malformation of aorta unspecified
  
*'''[[P23.3]]''' Congenital pneumonia due to streptococcus, group B
+
*'''[[Q25.41]]''' Absence and aplasia of aorta
  
*'''[[P23.4]]''' Congenital pneumonia due to Escherichia coli
+
*'''[[Q25.42]]''' Hypoplasia of aorta
  
*'''[[P23.5]]''' Congenital pneumonia due to Pseudomonas
+
*'''[[Q25.43]]''' Congenital aneurysm of aorta
  
*'''[[P23.6]]''' Congenital pneumonia due to other bacterial agents
+
Congenital aneurysm of aortic root
  
Congenital pneumonia due to Hemophilus influenzae
+
Congenital aneurysm of aortic sinus
  
Congenital pneumonia due to Klebsiella pneumoniae
+
*'''[[Q25.44]]''' Congenital dilation of aorta
  
Congenital pneumonia due to Mycoplasma
+
*'''[[Q25.45]]''' Double aortic arch
  
Congenital pneumonia due to Streptococcus, except group B ''Use additional''
+
Vascular ring of aorta
  
code (B95-B96) to identify organism
+
*'''[[Q25.46]]''' Tortuous aortic arch
  
*'''[[P23.8]]''' Congenital pneumonia due to other organisms
+
Persistent convolutions of aortic arch
  
*'''[[P23.9]]''' Congenital pneumonia, unspecified
+
*'''[[Q25.47]]''' Right aortic arch
  
*'''[[P24]]''' Neonatal aspiration
+
Persistent right aortic arch
  
''Includes''  
+
*'''[[Q25.48]]''' Anomalous origin of subclavian artery
  
aspiration in utero and during delivery
+
*'''[[Q25.49]]''' Other congenital malformations of aorta
  
*'''[[P24.0]]''' Meconium aspiration
+
Aortic arch
  
''Excludes1''
+
Bovine arch
  
meconium passage (without aspiration) during delivery (P03.82]]''' ) '''
+
*'''[[Q25.5]]''' Atresia of pulmonary artery
  
meconium staining (P96.83]]''' )'''
+
*'''[[Q25.6]]''' Stenosis of pulmonary artery
  
*'''[[P24.00]]''' Meconium aspiration without respiratory symptoms
+
Supravalvular pulmonary stenosis
  
Meconium aspiration NOS
+
*'''[[Q25.7]]''' Other congenital malformations of pulmonary artery
  
*'''[[P24.01]]''' Meconium aspiration with respiratory symptoms
+
*'''[[Q25.71]]''' Coarctation of pulmonary artery
  
Meconium aspiration pneumonia
+
*'''[[Q25.72]]''' Congenital pulmonary arteriovenous malformation
  
Meconium aspiration pneumonitis
+
Congenital pulmonary arteriovenous aneurysm
  
Meconium aspiration syndrome NOS ''Use additional''  
+
*'''[[Q25.79]]''' Other congenital malformations of pulmonary artery
  
code to identify any secondary pulmonary hypertension, if applicable (I27.2-)
+
Aberrant pulmonary artery
  
*'''[[P24.1]]''' Neonatal aspiration of (clear) amniotic fluid and mucus
+
Agenesis of pulmonary artery
  
Neonatal aspiration of liquor (amnii)
+
Congenital aneurysm of pulmonary artery
  
*'''[[P24.10]]''' Neonatal aspiration of (clear) amniotic fluid and mucus without respiratory symptoms
+
Congenital anomaly of pulmonary artery
  
Neonatal aspiration of amniotic fluid and mucus NOS
+
Hypoplasia of pulmonary artery
  
*'''[[P24.11]]''' Neonatal aspiration of (clear) amniotic fluid and mucus with respiratory symptoms
+
*'''[[Q25.8]]''' Other congenital malformations of other great arteries
  
Neonatal aspiration of amniotic fluid and mucus with pneumonia
+
*'''[[Q25.9]]''' Congenital malformation of great arteries, unspecified
  
Neonatal aspiration of amniotic fluid and mucus with pneumonitis ''Use additional''  
+
*'''[[Q26]]''' Congenital malformations of great veins
  
code to identify any secondary pulmonary hypertension, if applicable (I27.2-)
+
*'''[[Q26.0]]''' Congenital stenosis of vena cava
  
*'''[[P24.2]]''' Neonatal aspiration of blood
+
Congenital stenosis of vena cava (inferior)(superior)
  
*'''[[P24.20]]''' Neonatal aspiration of blood without respiratory symptoms
+
*'''[[Q26.1]]''' Persistent left superior vena cava
  
Neonatal aspiration of blood NOS
+
*'''[[Q26.2]]''' Total anomalous pulmonary venous connection
  
*'''[[P24.21]]''' Neonatal aspiration of blood with respiratory symptoms
+
Total anomalous pulmonary venous return (TAPVR), subdiaphragmatic
  
Neonatal aspiration of blood with pneumonia
+
Total anomalous pulmonary venous return (TAPVR), supradiaphragmatic
  
Neonatal aspiration of blood with pneumonitis ''Use additional''  
+
*'''[[Q26.3]]''' Partial anomalous pulmonary venous connection
  
code to identify any secondary pulmonary hypertension, if applicable (I27.2-)
+
Partial anomalous pulmonary venous return
  
*'''[[P24.3]]''' Neonatal aspiration of milk and regurgitated food
+
*'''[[Q26.4]]''' Anomalous pulmonary venous connection, unspecified
  
Neonatal aspiration of stomach contents
+
*'''[[Q26.5]]''' Anomalous portal venous connection
  
*'''[[P24.30]]''' Neonatal aspiration of milk and regurgitated food without respiratory symptoms
+
*'''[[Q26.6]]''' Portal vein-hepatic artery fistula
  
Neonatal aspiration of milk and regurgitated food NOS
+
*'''[[Q26.8]]''' Other congenital malformations of great veins
  
*'''[[P24.31]]''' Neonatal aspiration of milk and regurgitated food with respiratory symptoms
+
Absence of vena cava (inferior) (superior)
  
Neonatal aspiration of milk and regurgitated food with pneumonia
+
Azygos continuation of inferior vena cava
  
Neonatal aspiration of milk and regurgitated food with pneumonitis ''Use additional''
+
Persistent left posterior cardinal vein
  
code to identify any secondary pulmonary hypertension, if applicable (I27.2-)
+
Scimitar syndrome
  
*'''[[P24.8]]''' Other neonatal aspiration
+
*'''[[Q26.9]]''' Congenital malformation of great vein, unspecified
  
*'''[[P24.80]]''' Other neonatal aspiration without respiratory symptoms
+
Congenital anomaly of vena cava (inferior) (superior) NOS
  
Neonatal aspiration NEC
+
*'''[[Q27]]''' Other congenital malformations of peripheral vascular system
  
*'''[[P24.81]]''' Other neonatal aspiration with respiratory symptoms
+
''Excludes2''  
  
Neonatal aspiration pneumonia NEC
+
anomalies of cerebral and precerebral vessels (Q28.0-Q28.3)
  
Neonatal aspiration with pneumonitis NEC
+
anomalies of coronary vessels (Q24.5)
  
Neonatal aspiration with pneumonia NOS
+
anomalies of pulmonary artery (Q25.5-Q25.7)
  
Neonatal aspiration with pneumonitis NOS ''Use additional''
+
congenital retinal aneurysm (Q14.1)
  
code to identify any secondary pulmonary hypertension, if applicable (I27.2-)
+
hemangioma and lymphangioma (D18.-)
  
*'''[[P24.9]]''' Neonatal aspiration, unspecified
+
*'''[[Q27.0]]''' Congenital absence and hypoplasia of umbilical artery
  
*'''[[P25]]''' Interstitial emphysema and related conditions originating in the perinatal period
+
Single umbilical artery
  
*'''[[P25.0]]''' Interstitial emphysema originating in the perinatal period
+
*'''[[Q27.1]]''' Congenital renal artery stenosis
  
*'''[[P25.1]]''' Pneumothorax originating in the perinatal period
+
*'''[[Q27.2]]''' Other congenital malformations of renal artery
  
*'''[[P25.2]]''' Pneumomediastinum originating in the perinatal period
+
Congenital malformation of renal artery NOS
  
*'''[[P25.3]]''' Pneumopericardium originating in the perinatal period
+
Multiple renal arteries
  
*'''[[P25.8]]''' Other conditions related to interstitial emphysema originating in the perinatal period
+
*'''[[Q27.3]]''' Arteriovenous malformation (peripheral)
  
*'''[[P26]]''' Pulmonary hemorrhage originating in the perinatal period
+
Arteriovenous aneurysm
  
 
''Excludes1''  
 
''Excludes1''  
  
acute idiopathic hemorrhage in infants over 28 days old (R04.81)
+
acquired arteriovenous aneurysm (I77.0)  
  
*'''[[P26.0]]''' Tracheobronchial hemorrhage originating in the perinatal period
+
''Excludes2''  
  
*'''[[P26.1]]''' Massive pulmonary hemorrhage originating in the perinatal period
+
arteriovenous malformation of cerebral vessels (Q28.2)
  
*'''[[P26.8]]''' Other pulmonary hemorrhages originating in the perinatal period
+
arteriovenous malformation of precerebral vessels (Q28.0)
  
*'''[[P26.9]]''' Unspecified pulmonary hemorrhage originating in the perinatal period
+
*'''[[Q27.30]]''' Arteriovenous malformation, site unspecified
  
*'''[[P27]]''' Chronic respiratory disease originating in the perinatal period
+
*'''[[Q27.31]]''' Arteriovenous malformation of vessel of upper limb
  
''Excludes2''  
+
*'''[[Q27.32]]''' Arteriovenous malformation of vessel of lower limb
 +
 
 +
*'''[[Q27.33]]''' Arteriovenous malformation of digestive system vessel
  
respiratory distress of newborn (P22.0-P22.9)
+
*'''[[Q27.34]]''' Arteriovenous malformation of renal vessel
  
*'''[[P27.0]]''' Wilson-Mikity syndrome
+
*'''[[Q27.39]]''' Arteriovenous malformation, other site
  
'''Pulmonary dysmaturity'''
+
*'''[[Q27.4]]''' Congenital phlebectasia
  
*'''[[P27.1]]''' Bronchopulmonary dysplasia originating in the perinatal period
+
*'''[[Q27.8]]''' Other specified congenital malformations of peripheral vascular system
  
*'''[[P27.8]]''' Other chronic respiratory diseases originating in the perinatal period
+
Absence of peripheral vascular system
  
Congenital pulmonary fibrosis
+
Atresia of peripheral vascular system
  
Ventilator lung in newborn
+
Congenital aneurysm (peripheral)
  
*'''[[P27.9]]''' Unspecified chronic respiratory disease originating in the perinatal period
+
Congenital stricture, artery
  
*'''[[P28]]''' Other respiratory conditions originating in the perinatal period
+
Congenital varix
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital malformations of the respiratory system (Q30-Q34)
+
arteriovenous malformation (Q27.3-)
  
*'''[[P28.0]]''' Primary atelectasis of newborn
+
*'''[[Q27.9]]''' Congenital malformation of peripheral vascular system, unspecified
  
'''Primary failure to expand terminal respiratory units'''
+
Anomaly of artery or vein NOS
  
'''Pulmonary hypoplasia associated with short gestation'''
+
*'''[[Q28]]''' Other congenital malformations of circulatory system
  
'''Pulmonary immaturity NOS'''
+
''Excludes1''  
  
*'''[[P28.1]]''' Other and unspecified atelectasis of newborn
+
congenital aneurysm NOS (Q27.8)
  
*'''[[P28.10]]''' Unspecified atelectasis of newborn
+
congenital coronary aneurysm (Q24.5)
  
Atelectasis of newborn NOS
+
ruptured cerebral arteriovenous malformation (I60.8)
  
*'''[[P28.11]]''' Resorption atelectasis without respiratory distress syndrome
+
ruptured malformation of precerebral vessels (I72.0)
  
''Excludes1''  
+
''Excludes2''  
  
resorption atelectasis with respiratory distress syndrome (P22.0)
+
congenital peripheral aneurysm (Q27.8)  
  
*'''[[P28.19]]''' Other atelectasis of newborn
+
congenital pulmonary aneurysm (Q25.79)
  
'''Partial atelectasis of newborn'''
+
congenital retinal aneurysm (Q14.1)
  
Secondary atelectasis of newborn
+
*'''[[Q28.0]]''' Arteriovenous malformation of precerebral vessels
  
*'''[[P28.2]]''' Cyanotic attacks of newborn
+
Congenital arteriovenous precerebral aneurysm (nonruptured)
  
''Excludes1''  
+
*'''[[Q28.1]]''' Other malformations of precerebral vessels
  
apnea of newborn (P28.3-P28.4)
+
Congenital malformation of precerebral vessels NOS
  
*'''[[P28.3]]''' Primary sleep apnea of newborn
+
Congenital precerebral aneurysm (nonruptured)
  
Central sleep apnea of newborn
+
*'''[[Q28.2]]''' Arteriovenous malformation of cerebral vessels
  
Obstructive sleep apnea of newborn
+
Arteriovenous malformation of brain NOS
  
Sleep apnea of newborn NOS
+
Congenital arteriovenous cerebral aneurysm (nonruptured)
  
*'''[[P28.4]]''' Other apnea of newborn
+
*'''[[Q28.3]]''' Other malformations of cerebral vessels
  
Apnea of prematurity
+
Congenital cerebral aneurysm (nonruptured)
  
Obstructive apnea of newborn
+
Congenital malformation of cerebral vessels NOS
  
''Excludes1''
+
Developmental venous anomaly
  
obstructive sleep apnea of newborn (P28.3)
+
*'''[[Q28.8]]''' Other specified congenital malformations of circulatory system
  
*'''[[P28.5]]''' Respiratory failure of newborn
+
Congenital aneurysm, specified site NEC
  
''Excludes1''
+
Spinal vessel anomaly
  
respiratory arrest of newborn (P28.81)
+
*'''[[Q28.9]]''' Congenital malformation of circulatory system, unspecified
  
respiratory distress of newborn (P22.0-)
+
Congenital malformations of the respiratory system (Q30-Q34)
  
*'''[[P28.8]]''' Other specified respiratory conditions of newborn
+
*'''[[Q30]]''' Congenital malformations of nose
  
*'''[[P28.81]]''' Respiratory arrest of newborn
+
''Excludes1''  
  
*'''[[P28.89]]''' Other specified respiratory conditions of newborn
+
congenital deviation of nasal septum (Q67.4)
  
Congenital laryngeal stridor
+
*'''[[Q30.0]]''' Choanal atresia
  
Sniffles in newborn
+
Atresia of nares (anterior) (posterior)
  
Snuffles in newborn
+
Congenital stenosis of nares (anterior) (posterior)
  
''Excludes1''  
+
*'''[[Q30.1]]''' Agenesis and underdevelopment of nose
  
early congenital syphilitic rhinitis (A50.05)
+
Congenital absent of nose
  
*'''[[P28.9]]''' Respiratory condition of newborn, unspecified
+
*'''[[Q30.2]]''' Fissured, notched and cleft nose
  
Respiratory depression in newborn
+
*'''[[Q30.3]]''' Congenital perforated nasal septum
  
*'''[[P29]]''' Cardiovascular disorders originating in the perinatal period
+
*'''[[Q30.8]]''' Other congenital malformations of nose
  
''Excludes1''  
+
Accessory nose
 +
 
 +
Congenital anomaly of nasal sinus wall
 +
 
 +
*'''[[Q30.9]]''' Congenital malformation of nose, unspecified
  
congenital malformations of the circulatory system (Q20-Q28)
+
*'''[[Q31]]''' Congenital malformations of larynx
  
*'''[[P29.0]]''' Neonatal cardiac failure
+
''Excludes1''  
  
*'''[[P29.1]]''' Neonatal cardiac dysrhythmia
+
congenital laryngeal stridor NOS (P28.89)
  
*'''[[P29.11]]''' Neonatal tachycardia
+
*'''[[Q31.0]]''' Web of larynx
  
*'''[[P29.12]]''' Neonatal bradycardia
+
Glottic web of larynx
  
*'''[[P29.2]]''' Neonatal hypertension
+
Subglottic web of larynx
  
*'''[[P29.3]]''' Persistent fetal circulation
+
Web of larynx NOS
  
*'''[[P29.30]]''' Pulmonary hypertension of newborn
+
*'''[[Q31.1]]''' Congenital subglottic stenosis
  
'''Persistent pulmonary hypertension of newborn'''
+
*'''[[Q31.2]]''' Laryngeal hypoplasia
  
*'''[[P29.38]]''' Other persistent fetal circulation
+
*'''[[Q31.3]]''' Laryngocele
  
Delayed closure of ductus arteriosus
+
*'''[[Q31.5]]''' Congenital laryngomalacia
  
*'''[[P29.4]]''' Transient myocardial ischemia in newborn
+
*'''[[Q31.8]]''' Other congenital malformations of larynx
  
*'''[[P29.8]]''' Other cardiovascular disorders originating in the perinatal period
+
Absence of larynx
  
*'''[[P29.81]]''' Cardiac arrest of newborn
+
Agenesis of larynx
  
*'''[[P29.89]]''' Other cardiovascular disorders originating in the perinatal period
+
Atresia of larynx
  
*'''[[P29.9]]''' Cardiovascular disorder originating in the perinatal period, unspecified
+
Congenital cleft thyroid cartilage
  
Infections specific to the perinatal period (P35-P39)
+
Congenital fissure of epiglottis
  
Infections acquired in utero, during birth via the umbilicus, or during the first 28 days after birth
+
Congenital stenosis of larynx NEC
  
''Excludes2''
+
Posterior cleft of cricoid cartilage
  
asymptomatic human immunodeficiency virus (HIV) infection status (Z21)
+
*'''[[Q31.9]]''' Congenital malformation of larynx, unspecified
  
congenital gonococcal infection (A54.-)
+
*'''[[Q32]]''' Congenital malformations of trachea and bronchus
  
congenital pneumonia (P23.-)
+
''Excludes1''
  
congenital syphilis (A50.-)  
+
congenital bronchiectasis (Q33.4)
  
human immunodeficiency virus (HIV) disease (B20)
+
*'''[[Q32.0]]''' Congenital tracheomalacia
  
infant botulism (A48.51)
+
*'''[[Q32.1]]''' Other congenital malformations of trachea
  
infectious diseases not specific to the perinatal period (A00-B99, J09, J10.-)
+
Atresia of trachea
  
intestinal infectious disease (A00-A09)
+
Congenital anomaly of tracheal cartilage
  
laboratory evidence of human immunodeficiency virus (HIV) (R75)
+
Congenital dilatation of trachea
  
tetanus neonatorum (A33)
+
Congenital malformation of trachea
  
*'''[[P35]]''' Congenital viral diseases
+
Congenital stenosis of trachea
  
''Includes''
+
Congenital tracheocele
  
infections acquired in utero or during birth
+
*'''[[Q32.2]]''' Congenital bronchomalacia
  
*'''[[P35.0]]''' Congenital rubella syndrome
+
*'''[[Q32.3]]''' Congenital stenosis of bronchus
  
Congenital rubella pneumonitis
+
*'''[[Q32.4]]''' Other congenital malformations of bronchus
  
*'''[[P35.1]]''' Congenital cytomegalovirus infection
+
Absence of bronchus
  
*'''[[P35.2]]''' Congenital herpesviral (herpes simplex) infection
+
Agenesis of bronchus
  
*'''[[P35.3]]''' Congenital viral hepatitis
+
Atresia of bronchus
  
*'''[[P35.4]]''' Congenital Zika virus disease ''Use additional''
+
Congenital diverticulum of bronchus
  
code to identify manifestations of congenital Zika virus disease
+
Congenital malformation of bronchus NOS
  
*'''[[P35.8]]''' Other congenital viral diseases
+
*'''[[Q33]]''' Congenital malformations of lung
  
Congenital varicella (chickenpox)
+
*'''[[Q33.0]]''' Congenital cystic lung
  
*'''[[P35.9]]''' Congenital viral disease, unspecified
+
Congenital cystic lung disease  
  
*'''[[P36]]''' Bacterial sepsis of newborn
+
Congenital honeycomb lung
  
''Includes''
+
Congenital polycystic lung disease
  
congenital sepsis ''Use additional''  
+
''Excludes1''  
  
code(s), if applicable, to identify severe sepsis (R65.2-) and associated acute organ dysfunction(s)
+
cystic fibrosis (E84.0)  
  
*'''[[P36.0]]''' Sepsis of newborn due to streptococcus, group B
+
cystic lung disease, acquired or unspecified (J98.4)
  
*'''[[P36.1]]''' Sepsis of newborn due to other and unspecified streptococci
+
*'''[[Q33.1]]''' Accessory lobe of lung
  
*'''[[P36.10]]''' Sepsis of newborn due to unspecified streptococci
+
Azygos lobe (fissured), lung
  
*'''[[P36.19]]''' Sepsis of newborn due to other streptococci
+
*'''[[Q33.2]]''' Sequestration of lung
  
*'''[[P36.2]]''' Sepsis of newborn due to Staphylococcus aureus
+
*'''[[Q33.3]]''' Agenesis of lung
  
*'''[[P36.3]]''' Sepsis of newborn due to other and unspecified staphylococci
+
Congenital absence of lung (lobe)
  
*'''[[P36.30]]''' Sepsis of newborn due to unspecified staphylococci
+
*'''[[Q33.4]]''' Congenital bronchiectasis
  
*'''[[P36.39]]''' Sepsis of newborn due to other staphylococci
+
*'''[[Q33.5]]''' Ectopic tissue in lung
  
*'''[[P36.4]]''' Sepsis of newborn due to Escherichia coli
+
*'''[[Q33.6]]''' Congenital hypoplasia and dysplasia of lung
  
*'''[[P36.5]]''' Sepsis of newborn due to anaerobes
+
''Excludes1''  
  
*'''[[P36.8]]''' Other bacterial sepsis of newborn ''Use additional''
+
pulmonary hypoplasia associated with short gestation (P28.0)
  
code from category B96 to identify organism
+
*'''[[Q33.8]]''' Other congenital malformations of lung
  
*'''[[P36.9]]''' Bacterial sepsis of newborn, unspecified
+
*'''[[Q33.9]]''' Congenital malformation of lung, unspecified
  
*'''[[P37]]''' Other congenital infectious and parasitic diseases
+
*'''[[Q34]]''' Other congenital malformations of respiratory system
  
 
''Excludes2''  
 
''Excludes2''  
  
congenital syphilis (A50.-)  
+
congenital central alveolar hypoventilation syndrome (G47.35)
  
infectious neonatal diarrhea (A00-A09)
+
*'''[[Q34.0]]''' Anomaly of pleura
  
necrotizing enterocolitis in newborn (P77.-)
+
*'''[[Q34.1]]''' Congenital cyst of mediastinum
  
noninfectious neonatal diarrhea (P78.3)
+
*'''[[Q34.8]]''' Other specified congenital malformations of respiratory system
  
ophthalmia neonatorum due to gonococcus (A54.31)
+
Atresia of nasopharynx
  
tetanus neonatorum (A33)
+
*'''[[Q34.9]]''' Congenital malformation of respiratory system, unspecified
  
*'''[[P37.0]]''' Congenital tuberculosis
+
Congenital absence of respiratory system
  
*'''[[P37.1]]''' Congenital toxoplasmosis
+
Congenital anomaly of respiratory system NOS
  
Hydrocephalus due to congenital toxoplasmosis
+
Cleft lip and cleft palate (Q35-Q37) ''Use additional''
  
*'''[[P37.2]]''' Neonatal (disseminated) listeriosis
+
code to identify associated malformation of the nose (Q30.2)  
  
*'''[[P37.3]]''' Congenital falciparum malaria
+
''Excludes1''
  
*'''[[P37.4]]''' Other congenital malaria
+
Robin's syndrome (Q87.0)
  
*'''[[P37.5]]''' Neonatal candidiasis
+
*'''[[Q35]]''' Cleft palate
  
*'''[[P37.8]]''' Other specified congenital infectious and parasitic diseases
+
''Includes''  
  
*'''[[P37.9]]''' Congenital infectious or parasitic disease, unspecified
+
fissure of palate
  
*'''[[P38]]''' Omphalitis of newborn
+
palatoschisis
  
 
''Excludes1''  
 
''Excludes1''  
  
omphalitis not of newborn (L08.82)  
+
cleft palate with cleft lip (Q37.-)
  
tetanus omphalitis (A33)
+
*'''[[Q35.1]]''' Cleft hard palate
  
umbilical hemorrhage of newborn (P51.-)
+
*'''[[Q35.3]]''' Cleft soft palate
  
*'''[[P38.1]]''' Omphalitis with mild hemorrhage
+
*'''[[Q35.5]]''' Cleft hard palate with cleft soft palate
  
*'''[[P38.9]]''' Omphalitis without hemorrhage
+
*'''[[Q35.7]]''' Cleft uvula
  
Omphalitis of newborn NOS
+
*'''[[Q35.9]]''' Cleft palate, unspecified
  
*'''[[P39]]''' Other infections specific to the perinatal period ''Use additional''
+
Cleft palate NOS
  
code to identify organism or specific infection
+
*'''[[Q36]]''' Cleft lip
  
*'''[[P39.0]]''' Neonatal infective mastitis
+
''Includes''  
 
 
''Excludes1''
 
 
 
breast engorgement of newborn (P83.4)
 
  
noninfective mastitis of newborn (P83.4)
+
cheiloschisis
  
*'''[[P39.1]]''' Neonatal conjunctivitis and dacryocystitis
+
congenital fissure of lip
  
Neonatal chlamydial conjunctivitis
+
harelip
  
Ophthalmia neonatorum NOS
+
labium leporinum
  
 
''Excludes1''  
 
''Excludes1''  
  
gonococcal conjunctivitis (A54.31)
+
cleft lip with cleft palate (Q37.-)
  
*'''[[P39.2]]''' Intra-amniotic infection affecting newborn, not elsewhere classified
+
*'''[[Q36.0]]''' Cleft lip, bilateral
  
*'''[[P39.3]]''' Neonatal urinary tract infection
+
*'''[[Q36.1]]''' Cleft lip, median
  
*'''[[P39.4]]''' Neonatal skin infection
+
*'''[[Q36.9]]''' Cleft lip, unilateral
  
Neonatal pyoderma
+
Cleft lip NOS
  
''Excludes1''  
+
*'''[[Q37]]''' Cleft palate with cleft lip
  
pemphigus neonatorum (L00)
+
''Includes''
  
staphylococcal scalded skin syndrome (L00)
+
cheilopalatoschisis
  
*'''[[P39.8]]''' Other specified infections specific to the perinatal period
+
*'''[[Q37.0]]''' Cleft hard palate with bilateral cleft lip
  
*'''[[P39.9]]''' Infection specific to the perinatal period, unspecified
+
*'''[[Q37.1]]''' Cleft hard palate with unilateral cleft lip
  
Hemorrhagic and hematological disorders of newborn (P50-P61)
+
Cleft hard palate with cleft lip NOS
  
''Excludes1''  
+
*'''[[Q37.2]]''' Cleft soft palate with bilateral cleft lip
  
congenital stenosis and stricture of bile ducts (Q44.3)
+
*'''[[Q37.3]]''' Cleft soft palate with unilateral cleft lip
  
Crigler-Najjar syndrome (E80.5)
+
Cleft soft palate with cleft lip NOS
  
Dubin-Johnson syndrome (E80.6)
+
*'''[[Q37.4]]''' Cleft hard and soft palate with bilateral cleft lip
  
Gilbert syndrome (E80.4)
+
*'''[[Q37.5]]''' Cleft hard and soft palate with unilateral cleft lip
  
hereditary hemolytic anemias (D55-D58)
+
Cleft hard and soft palate with cleft lip NOS
  
*'''[[P50]]''' Newborn affected by intrauterine (fetal) blood loss
+
*'''[[Q37.8]]''' Unspecified cleft palate with bilateral cleft lip
  
''Excludes1''  
+
*'''[[Q37.9]]''' Unspecified cleft palate with unilateral cleft lip
  
congenital anemia from intrauterine (fetal) blood loss (P61.3)
+
Cleft palate with cleft lip NOS
  
*'''[[P50.0]]''' Newborn affected by intrauterine (fetal) blood loss from vasa previa
+
Other congenital malformations of the digestive system (Q38-Q45)
  
*'''[[P50.1]]''' Newborn affected by intrauterine (fetal) blood loss from ruptured cord
+
*'''[[Q38]]''' Other congenital malformations of tongue, mouth and pharynx
  
*'''[[P50.2]]''' Newborn affected by intrauterine (fetal) blood loss from placenta
+
''Excludes1''  
  
*'''[[P50.3]]''' Newborn affected by hemorrhage into co-twin
+
dentofacial anomalies (M26.-)
  
*'''[[P50.4]]''' Newborn affected by hemorrhage into maternal circulation
+
macrostomia (Q18.4)
  
*'''[[P50.5]]''' Newborn affected by intrauterine (fetal) blood loss from cut end of co-twin's cord
+
microstomia (Q18.5)
  
*'''[[P50.8]]''' Newborn affected by other intrauterine (fetal) blood loss
+
*'''[[Q38.0]]''' Congenital malformations of lips, not elsewhere classified
  
*'''[[P50.9]]''' Newborn affected by intrauterine (fetal) blood loss, unspecified
+
Congenital fistula of lip
  
Newborn affected by fetal hemorrhage NOS
+
Congenital malformation of lip NOS
  
*'''[[P51]]''' Umbilical hemorrhage of newborn
+
Van der Woude's syndrome
  
 
''Excludes1''  
 
''Excludes1''  
  
omphalitis with mild hemorrhage (P38.1)  
+
cleft lip (Q36.-)
 +
 
 +
cleft lip with cleft palate (Q37.-)  
  
umbilical hemorrhage from cut end of co-twins cord (P50.5)
+
macrocheilia (Q18.6)  
  
*'''[[P51.0]]''' Massive umbilical hemorrhage of newborn
+
microcheilia (Q18.7)
  
*'''[[P51.8]]''' Other umbilical hemorrhages of newborn
+
*'''[[Q38.1]]''' Ankyloglossia
  
Slipped umbilical ligature NOS
+
Tongue tie
  
*'''[[P51.9]]''' Umbilical hemorrhage of newborn, unspecified
+
*'''[[Q38.2]]''' Macroglossia
  
*'''[[P52]]''' Intracranial nontraumatic hemorrhage of newborn
+
Congenital hypertrophy of tongue
  
''Includes''  
+
*'''[[Q38.3]]''' Other congenital malformations of tongue
  
intracranial hemorrhage due to anoxia or hypoxia
+
Aglossia
  
''Excludes1''
+
Bifid tongue
  
intracranial hemorrhage due to birth injury (P10.-)
+
Congenital adhesion of tongue
  
intracranial hemorrhage due to other injury (S06.-)
+
Congenital fissure of tongue
  
*'''[[P52.0]]''' Intraventricular (nontraumatic) hemorrhage, grade 1, of newborn
+
Congenital malformation of tongue NOS
  
Subependymal hemorrhage (without intraventricular extension)
+
Double tongue
  
Bleeding into germinal matrix
+
Hypoglossia
  
*'''[[P52.1]]''' Intraventricular (nontraumatic) hemorrhage, grade 2, of newborn
+
Hypoplasia of tongue
  
Subependymal hemorrhage with intraventricular extension
+
Microglossia
  
Bleeding into ventricle
+
*'''[[Q38.4]]''' Congenital malformations of salivary glands and ducts
  
*'''[[P52.2]]''' Intraventricular (nontraumatic) hemorrhage, grade 3 and grade 4, of newborn
+
Atresia of salivary glands and ducts
  
*'''[[P52.21]]''' Intraventricular (nontraumatic) hemorrhage, grade 3, of newborn
+
Congenital absence of salivary glands and ducts
  
Subependymal hemorrhage with intraventricular extension with enlargement of ventricle
+
Congenital accessory salivary glands and ducts
  
*'''[[P52.22]]''' Intraventricular (nontraumatic) hemorrhage, grade 4, of newborn
+
Congenital fistula of salivary gland
  
Bleeding into cerebral cortex
+
*'''[[Q38.5]]''' Congenital malformations of palate, not elsewhere classified
  
Subependymal hemorrhage with intracerebral extension
+
Congenital absence of uvula
  
*'''[[P52.3]]''' Unspecified intraventricular (nontraumatic) hemorrhage of newborn
+
Congenital malformation of palate NOS
  
*'''[[P52.4]]''' Intracerebral (nontraumatic) hemorrhage of newborn
+
Congenital high arched palate
  
*'''[[P52.5]]''' Subarachnoid (nontraumatic) hemorrhage of newborn
+
''Excludes1''  
  
*'''[[P52.6]]''' Cerebellar (nontraumatic) and posterior fossa hemorrhage of newborn
+
cleft palate (Q35.-)  
  
*'''[[P52.8]]''' Other intracranial (nontraumatic) hemorrhages of newborn
+
cleft palate with cleft lip (Q37.-)
  
*'''[[P52.9]]''' Intracranial (nontraumatic) hemorrhage of newborn, unspecified
+
*'''[[Q38.6]]''' Other congenital malformations of mouth
  
*'''[[P53]]''' Hemorrhagic disease of newborn
+
Congenital malformation of mouth NOS
  
Vitamin K deficiency of newborn
+
*'''[[Q38.7]]''' Congenital pharyngeal pouch
  
*'''[[P54]]''' Other neonatal hemorrhages
+
Congenital diverticulum of pharynx
  
 
''Excludes1''  
 
''Excludes1''  
  
newborn affected by (intrauterine) blood loss (P50.-)  
+
pharyngeal pouch syndrome (D82.1)
  
pulmonary hemorrhage originating in the perinatal period (P26.-)
+
*'''[[Q38.8]]''' Other congenital malformations of pharynx
  
*'''[[P54.0]]''' Neonatal hematemesis
+
Congenital malformation of pharynx NOS
  
''Excludes1''
+
Imperforate pharynx
  
neonatal hematemesis due to swallowed maternal blood (P78.2)
+
*'''[[Q39]]''' Congenital malformations of esophagus
  
*'''[[P54.1]]''' Neonatal melena
+
*'''[[Q39.0]]''' Atresia of esophagus without fistula
  
''Excludes1''
+
Atresia of esophagus NOS
  
neonatal melena due to swallowed maternal blood (P78.2)
+
*'''[[Q39.1]]''' Atresia of esophagus with tracheo-esophageal fistula
  
*'''[[P54.2]]''' Neonatal rectal hemorrhage
+
Atresia of esophagus with broncho-esophageal fistula
  
*'''[[P54.3]]''' Other neonatal gastrointestinal hemorrhage
+
*'''[[Q39.2]]''' Congenital tracheo-esophageal fistula without atresia
  
*'''[[P54.4]]''' Neonatal adrenal hemorrhage
+
Congenital tracheo-esophageal fistula NOS
  
*'''[[P54.5]]''' Neonatal cutaneous hemorrhage
+
*'''[[Q39.3]]''' Congenital stenosis and stricture of esophagus
  
Neonatal bruising
+
*'''[[Q39.4]]''' Esophageal web
  
Neonatal ecchymoses
+
*'''[[Q39.5]]''' Congenital dilatation of esophagus
  
Neonatal petechiae
+
Congenital cardiospasm
  
Neonatal superficial hematomata
+
*'''[[Q39.6]]''' Congenital diverticulum of esophagus
  
''Excludes2''
+
Congenital esophageal pouch
  
bruising of scalp due to birth injury (P12.3)
+
*'''[[Q39.8]]''' Other congenital malformations of esophagus
  
cephalhematoma due to birth injury (P12.0)
+
Congenital absence of esophagus
  
*'''[[P54.6]]''' Neonatal vaginal hemorrhage
+
Congenital displacement of esophagus
  
Neonatal pseudomenses
+
Congenital duplication of esophagus
  
*'''[[P54.8]]''' Other specified neonatal hemorrhages
+
*'''[[Q39.9]]''' Congenital malformation of esophagus, unspecified
  
*'''[[P54.9]]''' Neonatal hemorrhage, unspecified
+
*'''[[Q40]]''' Other congenital malformations of upper alimentary tract
  
*'''[[P55]]''' Hemolytic disease of newborn
+
*'''[[Q40.0]]''' Congenital hypertrophic pyloric stenosis
  
*'''[[P55.0]]''' Rh isoimmunization of newborn
+
Congenital or infantile constriction
  
*'''[[P55.1]]''' ABO isoimmunization of newborn
+
Congenital or infantile hypertrophy
  
*'''[[P55.8]]''' Other hemolytic diseases of newborn
+
Congenital or infantile spasm
  
*'''[[P55.9]]''' Hemolytic disease of newborn, unspecified
+
Congenital or infantile stenosis
  
*'''[[P56]]''' Hydrops fetalis due to hemolytic disease
+
Congenital or infantile stricture
 +
 
 +
*'''[[Q40.1]]''' Congenital hiatus hernia
 +
 
 +
Congenital displacement of cardia through esophageal hiatus
  
 
''Excludes1''  
 
''Excludes1''  
  
hydrops fetalis NOS (P83.2)
+
congenital diaphragmatic hernia (Q79.0)
  
*'''[[P56.0]]''' Hydrops fetalis due to isoimmunization
+
*'''[[Q40.2]]''' Other specified congenital malformations of stomach
  
*'''[[P56.9]]''' Hydrops fetalis due to other and unspecified hemolytic disease
+
Congenital displacement of stomach
  
*'''[[P56.90]]''' Hydrops fetalis due to unspecified hemolytic disease
+
Congenital diverticulum of stomach
  
*'''[[P56.99]]''' Hydrops fetalis due to other hemolytic disease
+
Congenital hourglass stomach
  
*'''[[P57]]''' Kernicterus
+
Congenital duplication of stomach
  
*'''[[P57.0]]''' Kernicterus due to isoimmunization
+
Megalogastria
  
*'''[[P57.8]]''' Other specified kernicterus
+
Microgastria
  
''Excludes1''  
+
*'''[[Q40.3]]''' Congenital malformation of stomach, unspecified
  
Crigler-Najjar syndrome (E80.5)
+
*'''[[Q40.8]]''' Other specified congenital malformations of upper alimentary tract
  
*'''[[P57.9]]''' Kernicterus, unspecified
+
*'''[[Q40.9]]''' Congenital malformation of upper alimentary tract, unspecified
  
*'''[[P58]]''' Neonatal jaundice due to other excessive hemolysis
+
Congenital anomaly of upper alimentary tract
  
''Excludes1''
+
Congenital deformity of upper alimentary tract
  
jaundice due to isoimmunization (P55-P57)
+
*'''[[Q41]]''' Congenital absence, atresia and stenosis of small intestine
  
*'''[[P58.0]]''' Neonatal jaundice due to bruising
+
''Includes''  
  
*'''[[P58.1]]''' Neonatal jaundice due to bleeding
+
congenital obstruction, occlusion or stricture of small intestine or intestine NOS
  
*'''[[P58.2]]''' Neonatal jaundice due to infection
+
''Excludes1''  
 
 
*'''[[P58.3]]''' Neonatal jaundice due to polycythemia
 
  
*'''[[P58.4]]''' Neonatal jaundice due to drugs or toxins transmitted from mother or given to newborn ''Code first''
+
cystic fibrosis with intestinal manifestation (E84.11)
  
poisoning due to drug or toxin, if applicable (T36-T65 with fifth or sixth character 1-4 or 6) ''Use additional''
+
meconium ileus NOS (without cystic fibrosis) (P76.0)
  
code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
+
*'''[[Q41.0]]''' Congenital absence, atresia and stenosis of duodenum
  
*'''[[P58.41]]''' Neonatal jaundice due to drugs or toxins transmitted from mother
+
*'''[[Q41.1]]''' Congenital absence, atresia and stenosis of jejunum
  
*'''[[P58.42]]''' Neonatal jaundice due to drugs or toxins given to newborn
+
Apple peel syndrome
  
*'''[[P58.5]]''' Neonatal jaundice due to swallowed maternal blood
+
Imperforate jejunum
  
*'''[[P58.8]]''' Neonatal jaundice due to other specified excessive hemolysis
+
*'''[[Q41.2]]''' Congenital absence, atresia and stenosis of ileum
  
*'''[[P58.9]]''' Neonatal jaundice due to excessive hemolysis, unspecified
+
*'''[[Q41.8]]''' Congenital absence, atresia and stenosis of other specified parts of small intestine
  
*'''[[P59]]''' Neonatal jaundice from other and unspecified causes
+
*'''[[Q41.9]]''' Congenital absence, atresia and stenosis of small intestine, part unspecified
  
''Excludes1''
+
Congenital absence, atresia and stenosis of intestine NOS
  
jaundice due to inborn errors of metabolism (E70-E88)
+
*'''[[Q42]]''' Congenital absence, atresia and stenosis of large intestine
  
kernicterus (P57.-)
+
''Includes''
  
*'''[[P59.0]]''' Neonatal jaundice associated with preterm delivery
+
congenital obstruction, occlusion and stricture of large intestine
  
Hyperbilirubinemia of prematurity
+
*'''[[Q42.0]]''' Congenital absence, atresia and stenosis of rectum with fistula
  
Jaundice due to delayed conjugation associated with preterm delivery
+
*'''[[Q42.1]]''' Congenital absence, atresia and stenosis of rectum without fistula
  
*'''[[P59.1]]''' Inspissated bile syndrome
+
Imperforate rectum
  
*'''[[P59.2]]''' Neonatal jaundice from other and unspecified hepatocellular damage
+
*'''[[Q42.2]]''' Congenital absence, atresia and stenosis of anus with fistula
  
''Excludes1''  
+
*'''[[Q42.3]]''' Congenital absence, atresia and stenosis of anus without fistula
  
congenital viral hepatitis (P35.3)
+
Imperforate anus
  
*'''[[P59.20]]''' Neonatal jaundice from unspecified hepatocellular damage
+
*'''[[Q42.8]]''' Congenital absence, atresia and stenosis of other parts of large intestine
  
*'''[[P59.29]]''' Neonatal jaundice from other hepatocellular damage
+
*'''[[Q42.9]]''' Congenital absence, atresia and stenosis of large intestine, part unspecified
  
Neonatal giant cell hepatitis
+
*'''[[Q43]]''' Other congenital malformations of intestine
  
Neonatal (idiopathic) hepatitis
+
*'''[[Q43.0]]''' Meckel's diverticulum (displaced) (hypertrophic)
  
*'''[[P59.3]]''' Neonatal jaundice from breast milk inhibitor
+
Persistent omphalomesenteric duct
  
*'''[[P59.8]]''' Neonatal jaundice from other specified causes
+
Persistent vitelline duct
  
*'''[[P59.9]]''' Neonatal jaundice, unspecified
+
*'''[[Q43.1]]''' Hirschsprung's disease
  
Neonatal physiological jaundice (intense)(prolonged) NOS
+
Aganglionosis
  
*'''[[P60]]''' Disseminated intravascular coagulation of newborn
+
Congenital (aganglionic) megacolon
  
Defibrination syndrome of newborn
+
*'''[[Q43.2]]''' Other congenital functional disorders of colon
  
*'''[[P61]]''' Other perinatal hematological disorders
+
Congenital dilatation of colon
  
''Excludes1''  
+
*'''[[Q43.3]]''' Congenital malformations of intestinal fixation
  
transient hypogammaglobulinemia of infancy (D80.7)
+
Congenital omental, anomalous adhesions (bands)  
  
*'''[[P61.0]]''' Transient neonatal thrombocytopenia
+
Congenital peritoneal adhesions (bands)
  
Neonatal thrombocytopenia due to exchange transfusion
+
Incomplete rotation of cecum and colon
  
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia
+
Insufficient rotation of cecum and colon
  
Neonatal thrombocytopenia due to isoimmunization
+
Jackson's membrane
  
*'''[[P61.1]]''' Polycythemia neonatorum
+
Malrotation of colon
  
*'''[[P61.2]]''' Anemia of prematurity
+
Rotation failure of cecum and colon
  
*'''[[P61.3]]''' Congenital anemia from fetal blood loss
+
Universal mesentery
  
*'''[[P61.4]]''' Other congenital anemias, not elsewhere classified
+
*'''[[Q43.4]]''' Duplication of intestine
  
Congenital anemia NOS
+
*'''[[Q43.5]]''' Ectopic anus
  
*'''[[P61.5]]''' Transient neonatal neutropenia
+
*'''[[Q43.6]]''' Congenital fistula of rectum and anus
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital neutropenia (nontransient) (D70.0)
+
congenital fistula of anus with absence, atresia and stenosis (Q42.2)  
  
*'''[[P61.6]]''' Other transient neonatal disorders of coagulation
+
congenital fistula of rectum with absence, atresia and stenosis (Q42.0)
  
*'''[[P61.8]]''' Other specified perinatal hematological disorders
+
congenital rectovaginal fistula (Q52.2)
  
*'''[[P61.9]]''' Perinatal hematological disorder, unspecified
+
congenital urethrorectal fistula (Q64.73)
  
Transitory endocrine and metabolic disorders specific to newborn (P70-P74)  
+
pilonidal fistula or sinus (L05.-)
  
''Includes''  
+
*'''[[Q43.7]]''' Persistent cloaca
 +
 
 +
Cloaca NOS
  
transitory endocrine and metabolic disturbances caused by the infant's response to maternal endocrine and
+
*'''[[Q43.8]]''' Other specified congenital malformations of intestine
  
metabolic factors, or its adjustment to extrauterine environment
+
Congenital blind loop syndrome
  
*'''[[P70]]''' Transitory disorders of carbohydrate metabolism specific to newborn
+
Congenital diverticulitis, colon
  
*'''[[P70.0]]''' Syndrome of infant of mother with gestational diabetes
+
Congenital diverticulum, intestine
  
Newborn (with hypoglycemia) affected by maternal gestational diabetes
+
Dolichocolon
  
''Excludes1''
+
Megaloappendix
  
newborn (with hypoglycemia) affected by maternal (pre-existing) diabetes mellitus (P70.1)
+
Megaloduodenum
  
syndrome of infant of a diabetic mother (P70.1)
+
Microcolon
  
*'''[[P70.1]]''' Syndrome of infant of a diabetic mother
+
Transposition of appendix
  
Newborn (with hypoglycemia) affected by maternal (pre-existing) diabetes mellitus
+
Transposition of colon
  
''Excludes1''
+
Transposition of intestine
  
newborn (with hypoglycemia) affected by maternal gestational diabetes (P70.0)
+
*'''[[Q43.9]]''' Congenital malformation of intestine, unspecified
  
syndrome of infant of mother with gestational diabetes (P70.0)
+
*'''[[Q44]]''' Congenital malformations of gallbladder, bile ducts and liver
  
*'''[[P70.2]]''' Neonatal diabetes mellitus
+
*'''[[Q44.0]]''' Agenesis, aplasia and hypoplasia of gallbladder
  
*'''[[P70.3]]''' Iatrogenic neonatal hypoglycemia
+
Congenital absence of gallbladder
  
*'''[[P70.4]]''' Other neonatal hypoglycemia
+
*'''[[Q44.1]]''' Other congenital malformations of gallbladder
  
Transitory neonatal hypoglycemia
+
Congenital malformation of gallbladder NOS
  
*'''[[P70.8]]''' Other transitory disorders of carbohydrate metabolism of newborn
+
Intrahepatic gallbladder
  
*'''[[P70.9]]''' Transitory disorder of carbohydrate metabolism of newborn, unspecified
+
*'''[[Q44.2]]''' Atresia of bile ducts
  
*'''[[P71]]''' Transitory neonatal disorders of calcium and magnesium metabolism
+
*'''[[Q44.3]]''' Congenital stenosis and stricture of bile ducts
  
*'''[[P71.0]]''' Cow's milk hypocalcemia in newborn
+
*'''[[Q44.4]]''' Choledochal cyst
  
*'''[[P71.1]]''' Other neonatal hypocalcemia
+
*'''[[Q44.5]]''' Other congenital malformations of bile ducts
  
''Excludes1''
+
Accessory hepatic duct
  
neonatal hypoparathyroidism (P71.4)
+
Biliary duct duplication
  
*'''[[P71.2]]''' Neonatal hypomagnesemia
+
Congenital malformation of bile duct NOS
  
*'''[[P71.3]]''' Neonatal tetany without calcium or magnesium deficiency
+
Cystic duct duplication
  
Neonatal tetany NOS
+
*'''[[Q44.6]]''' Cystic disease of liver
  
*'''[[P71.4]]''' Transitory neonatal hypoparathyroidism
+
Fibrocystic disease of liver
  
*'''[[P71.8]]''' Other transitory neonatal disorders of calcium and magnesium metabolism
+
*'''[[Q44.7]]''' Other congenital malformations of liver
  
*'''[[P71.9]]''' Transitory neonatal disorder of calcium and magnesium metabolism, unspecified
+
Accessory liver
  
*'''[[P72]]''' Other transitory neonatal endocrine disorders
+
Alagille's syndrome
  
''Excludes1''
+
Congenital absence of liver
  
congenital hypothyroidism with or without goiter (E03.0-E03.1)
+
Congenital hepatomegaly
  
dyshormogenetic goiter (E07.1)
+
Congenital malformation of liver NOS
  
'''Pendred's syndrome (E07.1)'''
+
*'''[[Q45]]''' Other congenital malformations of digestive system
  
*'''[[P72.0]]''' Neonatal goiter, not elsewhere classified
+
''Excludes2''  
  
Transitory congenital goiter with normal functioning
+
congenital diaphragmatic hernia (Q79.0)
  
*'''[[P72.1]]''' Transitory neonatal hyperthyroidism
+
congenital hiatus hernia (Q40.1)
  
Neonatal thyrotoxicosis
+
*'''[[Q45.0]]''' Agenesis, aplasia and hypoplasia of pancreas
  
*'''[[P72.2]]''' Other transitory neonatal disorders of thyroid function, not elsewhere classified
+
Congenital absence of pancreas
  
Transitory neonatal hypothyroidism
+
*'''[[Q45.1]]''' Annular pancreas
  
*'''[[P72.8]]''' Other specified transitory neonatal endocrine disorders
+
*'''[[Q45.2]]''' Congenital pancreatic cyst
  
*'''[[P72.9]]''' Transitory neonatal endocrine disorder, unspecified
+
*'''[[Q45.3]]''' Other congenital malformations of pancreas and pancreatic duct
  
*'''[[P74]]''' Other transitory neonatal electrolyte and metabolic disturbances
+
Accessory pancreas
  
*'''[[P74.0]]''' Late metabolic acidosis of newborn
+
Congenital malformation of pancreas or pancreatic duct NOS
  
 
''Excludes1''  
 
''Excludes1''  
  
(fetal) metabolic acidosis of newborn (P19)
+
congenital diabetes mellitus (E10.-)  
  
*'''[[P74.1]]''' Dehydration of newborn
+
cystic fibrosis (E84.0-E84.9)
  
*'''[[P74.2]]''' Disturbances of sodium balance of newborn
+
fibrocystic disease of pancreas (E84.-)
  
*'''[[P74.21]]''' Hypernatremia of newborn
+
neonatal diabetes mellitus (P70.2)
  
*'''[[P74.22]]''' Hyponatremia of newborn
+
*'''[[Q45.8]]''' Other specified congenital malformations of digestive system
  
*'''[[P74.3]]''' Disturbances of potassium balance of newborn
+
Absence (complete) (partial) of alimentary tract NOS
  
*'''[[P74.31]]''' Hyperkalemia of newborn
+
Duplication of digestive system
  
*'''[[P74.32]]''' Hypokalemia of newborn
+
Malposition, congenital of digestive system
  
*'''[[P74.4]]''' Other transitory electrolyte disturbances of newborn
+
*'''[[Q45.9]]''' Congenital malformation of digestive system, unspecified
  
*'''[[P74.41]]''' Alkalosis of newborn
+
Congenital anomaly of digestive system
  
Hyperbicarbonatemia
+
Congenital deformity of digestive system
  
*'''[[P74.42]]''' Disturbances of chlorine balance of newborn
+
Congenital malformations of genital organs (Q50-Q56)
  
*'''[[P74.421]]''' Hyperchloremia of newborn
+
''Excludes1''  
  
Hyperchloremic metabolic acidosis
+
androgen insensitivity syndrome (E34.5-)
  
''Excludes2''
+
syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)
  
late metabolic acidosis of the newborn (P74.0)
+
*'''[[Q50]]''' Congenital malformations of ovaries, fallopian tubes and broad ligaments
  
*'''[[P74.422]]''' Hypochloremia of newborn
+
*'''[[Q50.0]]''' Congenital absence of ovary
  
*'''[[P74.49]]''' Other transitory electrolyte disturbance of newborn
+
''Excludes1''
  
*'''[[P74.5]]''' Transitory tyrosinemia of newborn
+
Turner's syndrome (Q96.-)
  
*'''[[P74.6]]''' Transitory hyperammonemia of newborn
+
*'''[[Q50.01]]''' Congenital absence of ovary, unilateral
  
*'''[[P74.8]]''' Other transitory metabolic disturbances of newborn
+
*'''[[Q50.02]]''' Congenital absence of ovary, bilateral
  
Amino-acid metabolic disorders described as transitory
+
*'''[[Q50.1]]''' Developmental ovarian cyst
  
*'''[[P74.9]]''' Transitory metabolic disturbance of newborn, unspecified
+
*'''[[Q50.2]]''' Congenital torsion of ovary
  
Digestive system disorders of newborn (P76-P78)
+
*'''[[Q50.3]]''' Other congenital malformations of ovary
  
*'''[[P76]]''' Other intestinal obstruction of newborn
+
*'''[[Q50.31]]''' Accessory ovary
  
*'''[[P76.0]]''' Meconium plug syndrome
+
*'''[[Q50.32]]''' Ovarian streak
  
Meconium ileus NOS
+
46, XX with streak gonads
  
''Excludes1''  
+
*'''[[Q50.39]]''' Other congenital malformation of ovary
  
meconium ileus in cystic fibrosis (E84.11)
+
Congenital malformation of ovary NOS
  
*'''[[P76.1]]''' Transitory ileus of newborn
+
*'''[[Q50.4]]''' Embryonic cyst of fallopian tube
  
''Excludes1''
+
Fimbrial cyst
  
Hirschsprung's disease (Q43.1)
+
*'''[[Q50.5]]''' Embryonic cyst of broad ligament
  
*'''[[P76.2]]''' Intestinal obstruction due to inspissated milk
+
Epoophoron cyst
  
*'''[[P76.8]]''' Other specified intestinal obstruction of newborn
+
Parovarian cyst
  
''Excludes1''  
+
*'''[[Q50.6]]''' Other congenital malformations of fallopian tube and broad ligament
  
intestinal obstruction classifiable to K56.-
+
Absence of fallopian tube and broad ligament
  
*'''[[P76.9]]''' Intestinal obstruction of newborn, unspecified
+
Accessory fallopian tube and broad ligament
  
*'''[[P77]]''' Necrotizing enterocolitis of newborn
+
Atresia of fallopian tube and broad ligament
  
*'''[[P77.1]]''' Stage 1 necrotizing enterocolitis in newborn
+
Congenital malformation of fallopian tube or broad ligament NOS
  
Necrotizing enterocolitis without pneumatosis, without perforation
+
*'''[[Q51]]''' Congenital malformations of uterus and cervix
  
*'''[[P77.2]]''' Stage 2 necrotizing enterocolitis in newborn
+
*'''[[Q51.0]]''' Agenesis and aplasia of uterus
  
Necrotizing enterocolitis with pneumatosis, without perforation
+
Congenital absence of uterus
  
*'''[[P77.3]]''' Stage 3 necrotizing enterocolitis in newborn
+
*'''[[Q51.1]]''' Doubling of uterus with doubling of cervix and vagina
  
Necrotizing enterocolitis with perforation
+
*'''[[Q51.10]]''' Doubling of uterus with doubling of cervix and vagina without obstruction
  
Necrotizing enterocolitis with pneumatosis and perforation
+
Doubling of uterus with doubling of cervix and vagina NOS
  
*'''[[P77.9]]''' Necrotizing enterocolitis in newborn, unspecified
+
*'''[[Q51.11]]''' Doubling of uterus with doubling of cervix and vagina with obstruction
  
Necrotizing enterocolitis in newborn, NOS
+
*'''[[Q51.2]]''' Other doubling of uterus
  
*'''[[P78]]''' Other perinatal digestive system disorders
+
Doubling of uterus NOS
  
''Excludes1''
+
Septate uterus
  
cystic fibrosis (E84.0-E84.9)
+
*'''[[Q51.20]]''' Other doubling of uterus, unspecified
  
neonatal gastrointestinal hemorrhages (P54.0-P54.3)
+
Septate uterus, unspecified
  
*'''[[P78.0]]''' Perinatal intestinal perforation
+
*'''[[Q51.21]]''' Other complete doubling of uterus
  
Meconium peritonitis
+
Complete septate uterus
  
*'''[[P78.1]]''' Other neonatal peritonitis
+
*'''[[Q51.22]]''' Other partial doubling of uterus
  
Neonatal peritonitis NOS
+
Partial septate uterus
  
*'''[[P78.2]]''' Neonatal hematemesis and melena due to swallowed maternal blood
+
*'''[[Q51.28]]''' Other doubling of uterus, other specified
  
*'''[[P78.3]]''' Noninfective neonatal diarrhea
+
Septate uterus, other specified
  
Neonatal diarrhea NOS
+
*'''[[Q51.3]]''' Bicornate uterus
  
*'''[[P78.8]]''' Other specified perinatal digestive system disorders
+
Bicornate uterus, complete or partial
  
*'''[[P78.81]]''' Congenital cirrhosis (of liver)
+
*'''[[Q51.4]]''' Unicornate uterus
  
*'''[[P78.82]]''' Peptic ulcer of newborn
+
Unicornate uterus with or without a separate uterine horn
  
*'''[[P78.83]]''' Newborn esophageal reflux
+
Uterus with only one functioning horn
  
Neonatal esophageal reflux
+
*'''[[Q51.5]]''' Agenesis and aplasia of cervix
  
*'''[[P78.84]]''' Gestational alloimmune liver disease
+
Congenital absence of cervix
  
GALD
+
*'''[[Q51.6]]''' Embryonic cyst of cervix
  
Neonatal hemochromatosis
+
*'''[[Q51.7]]''' Congenital fistulae between uterus and digestive and urinary tracts
  
''Excludes1''  
+
*'''[[Q51.8]]''' Other congenital malformations of uterus and cervix
  
hemochromatosis (E83.11-)
+
*'''[[Q51.81]]''' Other congenital malformations of uterus
  
*'''[[P78.89]]''' Other specified perinatal digestive system disorders
+
*'''[[Q51.810]]''' Arcuate uterus
  
*'''[[P78.9]]''' Perinatal digestive system disorder, unspecified
+
Arcuatus uterus
  
Conditions involving the integument and temperature regulation of newborn (P80-P83)
+
*'''[[Q51.811]]''' Hypoplasia of uterus
  
*'''[[P80]]''' Hypothermia of newborn
+
*'''[[Q51.818]]''' Other congenital malformations of uterus
  
*'''[[P80.0]]''' Cold injury syndrome
+
Müllerian anomaly of uterus NEC
  
Severe and usually chronic hypothermia associated with a pink flushed appearance, edema and neurological
+
*'''[[Q51.82]]''' Other congenital malformations of cervix
  
and biochemical abnormalities
+
*'''[[Q51.820]]''' Cervical duplication
  
''Excludes1''  
+
*'''[[Q51.821]]''' Hypoplasia of cervix
 +
 
 +
*'''[[Q51.828]]''' Other congenital malformations of cervix
 +
 
 +
*'''[[Q51.9]]''' Congenital malformation of uterus and cervix, unspecified
 +
 
 +
*'''[[Q52]]''' Other congenital malformations of female genitalia
 +
 
 +
*'''[[Q52.0]]''' Congenital absence of vagina
 +
 
 +
Vaginal agenesis, total or partial
  
mild hypothermia of newborn (P80.8)
+
*'''[[Q52.1]]''' Doubling of vagina
  
*'''[[P80.8]]''' Other hypothermia of newborn
+
''Excludes1''  
  
Mild hypothermia of newborn
+
doubling of vagina with doubling of uterus and cervix (Q51.1-)
  
*'''[[P80.9]]''' Hypothermia of newborn, unspecified
+
*'''[[Q52.10]]''' Doubling of vagina, unspecified
  
*'''[[P81]]''' Other disturbances of temperature regulation of newborn
+
Septate vagina NOS
  
*'''[[P81.0]]''' Environmental hyperthermia of newborn
+
*'''[[Q52.11]]''' Transverse vaginal septum
  
*'''[[P81.8]]''' Other specified disturbances of temperature regulation of newborn
+
*'''[[Q52.12]]''' Longitudinal vaginal septum
  
*'''[[P81.9]]''' Disturbance of temperature regulation of newborn, unspecified
+
*'''[[Q52.120]]''' Longitudinal vaginal septum, nonobstructing
  
Fever of newborn NOS
+
*'''[[Q52.121]]''' Longitudinal vaginal septum, obstructing, right side
  
*'''[[P83]]''' Other conditions of integument specific to newborn
+
*'''[[Q52.122]]''' Longitudinal vaginal septum, obstructing, left side
  
''Excludes1''  
+
*'''[[Q52.123]]''' Longitudinal vaginal septum, microperforate, right side
  
congenital malformations of skin and integument (Q80-Q84)
+
*'''[[Q52.124]]''' Longitudinal vaginal septum, microperforate, left side
  
hydrops fetalis due to hemolytic disease (P56.-)
+
*'''[[Q52.129]]''' Other and unspecified longitudinal vaginal septum
  
neonatal skin infection (P39.4)
+
*'''[[Q52.2]]''' Congenital rectovaginal fistula
  
staphylococcal scalded skin syndrome (L00)
+
''Excludes1''
  
''Excludes2''
+
cloaca (Q43.7)
  
cradle cap (L21.0)
+
*'''[[Q52.3]]''' Imperforate hymen
  
diaper (napkin) dermatitis (L22)
+
*'''[[Q52.4]]''' Other congenital malformations of vagina
  
*'''[[P83.0]]''' Sclerema neonatorum
+
Canal of Nuck cyst, congenital
  
*'''[[P83.1]]''' Neonatal erythema toxicum
+
Congenital malformation of vagina NOS
  
*'''[[P83.2]]''' Hydrops fetalis not due to hemolytic disease
+
Embryonic vaginal cyst
  
Hydrops fetalis NOS
+
Gartner's duct cyst
  
*'''[[P83.3]]''' Other and unspecified edema specific to newborn
+
*'''[[Q52.5]]''' Fusion of labia
  
*'''[[P83.30]]''' Unspecified edema specific to newborn
+
*'''[[Q52.6]]''' Congenital malformation of clitoris
  
*'''[[P83.39]]''' Other edema specific to newborn
+
*'''[[Q52.7]]''' Other and unspecified congenital malformations of vulva
  
*'''[[P83.4]]''' Breast engorgement of newborn
+
*'''[[Q52.70]]''' Unspecified congenital malformations of vulva
  
Noninfective mastitis of newborn
+
Congenital malformation of vulva NOS
  
*'''[[P83.5]]''' Congenital hydrocele
+
*'''[[Q52.71]]''' Congenital absence of vulva
  
*'''[[P83.6]]''' Umbilical polyp of newborn
+
*'''[[Q52.79]]''' Other congenital malformations of vulva
  
*'''[[P83.8]]''' Other specified conditions of integument specific to newborn
+
Congenital cyst of vulva
  
*'''[[P83.81]]''' Umbilical granuloma
+
*'''[[Q52.8]]''' Other specified congenital malformations of female genitalia
  
''Excludes2''  
+
*'''[[Q52.9]]''' Congenital malformation of female genitalia, unspecified
  
Granulomatous disorder of the skin and subcutaneous tissue, unspecified (L92.9)
+
*'''[[Q53]]''' Undescended and ectopic testicle
  
*'''[[P83.88]]''' Other specified conditions of integument specific to newborn
+
*'''[[Q53.0]]''' Ectopic testis
  
Bronze baby syndrome
+
*'''[[Q53.00]]''' Ectopic testis, unspecified
  
Neonatal scleroderma
+
*'''[[Q53.01]]''' Ectopic testis, unilateral
  
Urticaria neonatorum
+
*'''[[Q53.02]]''' Ectopic testes, bilateral
  
*'''[[P83.9]]''' Condition of the integument specific to newborn, unspecified
+
*'''[[Q53.1]]''' Undescended testicle, unilateral
  
Other problems with newborn (P84)
+
*'''[[Q53.10]]''' Unspecified undescended testicle, unilateral
  
*'''[[P84]]''' Other problems with newborn
+
*'''[[Q53.11]]''' Abdominal testis, unilateral
  
Acidemia of newborn
+
*'''[[Q53.111]]''' Unilateral intraabdominal testis
  
Acidosis of newborn
+
*'''[[Q53.112]]''' Unilateral inguinal testis
  
Anoxia of newborn NOS
+
*'''[[Q53.12]]''' Ectopic perineal testis, unilateral
  
Asphyxia of newborn NOS
+
*'''[[Q53.13]]''' Unilateral high scrotal testis
  
Hypercapnia of newborn
+
*'''[[Q53.2]]''' Undescended testicle, bilateral
  
Hypoxemia of newborn
+
*'''[[Q53.20]]''' Undescended testicle, unspecified, bilateral
  
Hypoxia of newborn NOS
+
*'''[[Q53.21]]''' Abdominal testis, bilateral
  
Mixed metabolic and respiratory acidosis of newborn
+
*'''[[Q53.211]]''' Bilateral intraabdominal testes
  
''Excludes1''  
+
*'''[[Q53.212]]''' Bilateral inguinal testes
  
intracranial hemorrhage due to anoxia or hypoxia (P52.-)
+
*'''[[Q53.22]]''' Ectopic perineal testis, bilateral
  
hypoxic ischemic encephalopathy (HIE) (P91.6-)
+
*'''[[Q53.23]]''' Bilateral high scrotal testes
  
late metabolic acidosis of newborn (P74.0)
+
*'''[[Q53.9]]''' Undescended testicle, unspecified
  
Other disorders originating in the perinatal period (P90-P96)
+
Cryptorchism NOS
  
*'''[[P90]]''' Convulsions of newborn
+
*'''[[Q54]]''' Hypospadias
  
 
''Excludes1''  
 
''Excludes1''  
  
benign myoclonic epilepsy in infancy (G40.3-)  
+
epispadias (Q64.0)
  
benign neonatal convulsions (familial) (G40.3-)
+
*'''[[Q54.0]]''' Hypospadias, balanic
  
*'''[[P91]]''' Other disturbances of cerebral status of newborn
+
Hypospadias, coronal
  
*'''[[P91.0]]''' Neonatal cerebral ischemia
+
Hypospadias, glandular
  
*'''[[P91.1]]''' Acquired periventricular cysts of newborn
+
*'''[[Q54.1]]''' Hypospadias, penile
  
*'''[[P91.2]]''' Neonatal cerebral leukomalacia
+
*'''[[Q54.2]]''' Hypospadias, penoscrotal
  
'''Periventricular leukomalacia'''
+
*'''[[Q54.3]]''' Hypospadias, perineal
  
*'''[[P91.3]]''' Neonatal cerebral irritability
+
*'''[[Q54.4]]''' Congenital chordee
  
*'''[[P91.4]]''' Neonatal cerebral depression
+
Chordee without hypospadias
  
*'''[[P91.5]]''' Neonatal coma
+
*'''[[Q54.8]]''' Other hypospadias
  
*'''[[P91.6]]''' Hypoxic ischemic encephalopathy (HIE)
+
Hypospadias with intersex state
  
''Excludes1''
+
*'''[[Q54.9]]''' Hypospadias, unspecified
  
Neonatal cerebral depression (P91.4)
+
*'''[[Q55]]''' Other congenital malformations of male genital organs
  
Neonatal cerebral irritability (P91.3)
+
''Excludes1''
 
 
Neonatal coma (P91.5)
 
  
*'''[[P91.60]]''' Hypoxic ischemic encephalopathy (HIE), unspecified
+
congenital hydrocele (P83.5)  
  
*'''[[P91.61]]''' Mild hypoxic ischemic encephalopathy (HIE)
+
hypospadias (Q54.-)
  
*'''[[P91.62]]''' Moderate hypoxic ischemic encephalopathy (HIE)
+
*'''[[Q55.0]]''' Absence and aplasia of testis
  
*'''[[P91.63]]''' Severe hypoxic ischemic encephalopathy (HIE)
+
Monorchism
  
*'''[[P91.8]]''' Other specified disturbances of cerebral status of newborn
+
*'''[[Q55.1]]''' Hypoplasia of testis and scrotum
  
*'''[[P91.81]]''' Neonatal encephalopathy
+
Fusion of testes
  
*'''[[P91.811]]''' Neonatal encephalopathy in diseases classified elsewhere ''Code first''
+
*'''[[Q55.2]]''' Other and unspecified congenital malformations of testis and scrotum
  
underlying condition, if known, such as
+
*'''[[Q55.20]]''' Unspecified congenital malformations of testis and scrotum
  
congenital cirrhosis (of liver) (P78.81)
+
Congenital malformation of testis or scrotum NOS
  
intracranial nontraumatic hemorrhage of newborn (P52.-)
+
*'''[[Q55.21]]''' Polyorchism
  
kernicterus (P57.-)
+
*'''[[Q55.22]]''' Retractile testis
  
*'''[[P91.819]]''' Neonatal encephalopathy, unspecified
+
*'''[[Q55.23]]''' Scrotal transposition
  
*'''[[P91.88]]''' Other specified disturbances of cerebral status of newborn
+
*'''[[Q55.29]]''' Other congenital malformations of testis and scrotum
  
*'''[[P91.9]]''' Disturbance of cerebral status of newborn, unspecified
+
*'''[[Q55.3]]''' Atresia of vas deferens ''Code first''
  
*'''[[P92]]''' Feeding problems of newborn
+
any associated cystic fibrosis (E84.-)
  
''Excludes1''  
+
*'''[[Q55.4]]''' Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
  
eating disorders (F50.-)
+
Absence or aplasia of prostate
  
feeding problems in child over 28 days old (R63.3)
+
Absence or aplasia of spermatic cord
  
*'''[[P92.0]]''' Vomiting of newborn
+
Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS
  
''Excludes1''  
+
*'''[[Q55.5]]''' Congenital absence and aplasia of penis
  
vomiting of child over 28 days old (R11.-)
+
*'''[[Q55.6]]''' Other congenital malformations of penis
  
*'''[[P92.01]]''' Bilious vomiting of newborn
+
*'''[[Q55.61]]''' Curvature of penis (lateral)
  
''Excludes1''  
+
*'''[[Q55.62]]''' Hypoplasia of penis
  
bilious vomiting in child over 28 days old (R11.14)
+
Micropenis
  
*'''[[P92.09]]''' Other vomiting of newborn
+
*'''[[Q55.63]]''' Congenital torsion of penis
  
 
''Excludes1''  
 
''Excludes1''  
  
regurgitation of food in newborn (P92.1)
+
acquired torsion of penis (N48.82)
  
*'''[[P92.1]]''' Regurgitation and rumination of newborn
+
*'''[[Q55.64]]''' Hidden penis
  
*'''[[P92.2]]''' Slow feeding of newborn
+
Buried penis
  
*'''[[P92.3]]''' Underfeeding of newborn
+
Concealed penis
  
*'''[[P92.4]]''' Overfeeding of newborn
+
''Excludes1''  
  
*'''[[P92.5]]''' Neonatal difficulty in feeding at breast
+
acquired buried penis (N48.83)
  
*'''[[P92.6]]''' Failure to thrive in newborn
+
*'''[[Q55.69]]''' Other congenital malformation of penis
  
''Excludes1''
+
Congenital malformation of penis NOS
  
failure to thrive in child over 28 days old (R62.51)
+
*'''[[Q55.7]]''' Congenital vasocutaneous fistula
  
*'''[[P92.8]]''' Other feeding problems of newborn
+
*'''[[Q55.8]]''' Other specified congenital malformations of male genital organs
  
*'''[[P92.9]]''' Feeding problem of newborn, unspecified
+
*'''[[Q55.9]]''' Congenital malformation of male genital organ, unspecified
  
*'''[[P93]]''' Reactions and intoxications due to drugs administered to newborn
+
Congenital anomaly of male genital organ
  
''Includes''
+
Congenital deformity of male genital organ
  
reactions and intoxications due to drugs administered to fetus affecting newborn
+
*'''[[Q56]]''' Indeterminate sex and pseudohermaphroditism
  
 
''Excludes1''  
 
''Excludes1''  
  
jaundice due to drugs or toxins transmitted from mother or given to newborn (P58.4-)  
+
46,XX true hermaphrodite (Q99.1)  
  
reactions and intoxications from maternal opiates, tranquilizers and other medication (P04.0-P04.1,
+
androgen insensitivity syndrome (E34.5-)
  
*'''[[P04.4-]]'''
+
chimera 46,XX/46,XY true hermaphrodite (Q99.0)
  
withdrawal symptoms from maternal use of drugs of addiction (P96.1)  
+
female pseudohermaphroditism with adrenocortical disorder (E25.-)  
  
withdrawal symptoms from therapeutic use of drugs in newborn (P96.2)
+
pseudohermaphroditism with specified chromosomal anomaly (Q96-Q99)  
  
*'''[[P93.0]]''' Grey baby syndrome
+
pure gonadal dysgenesis (Q99.1)
  
Grey syndrome from chloramphenicol administration in newborn
+
*'''[[Q56.0]]''' Hermaphroditism, not elsewhere classified
  
*'''[[P93.8]]''' Other reactions and intoxications due to drugs administered to newborn ''Use additional''
+
Ovotestis
  
code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
+
*'''[[Q56.1]]''' Male pseudohermaphroditism, not elsewhere classified
  
*'''[[P94]]''' Disorders of muscle tone of newborn
+
46, XY with streak gonads
  
*'''[[P94.0]]''' Transient neonatal myasthenia gravis
+
Male pseudohermaphroditism NOS
  
''Excludes1''  
+
*'''[[Q56.2]]''' Female pseudohermaphroditism, not elsewhere classified
  
myasthenia gravis (G70.0)
+
Female pseudohermaphroditism NOS
  
*'''[[P94.1]]''' Congenital hypertonia
+
*'''[[Q56.3]]''' Pseudohermaphroditism, unspecified
  
*'''[[P94.2]]''' Congenital hypotonia
+
*'''[[Q56.4]]''' Indeterminate sex, unspecified
  
Floppy baby syndrome, unspecified
+
Ambiguous genitalia
  
*'''[[P94.8]]''' Other disorders of muscle tone of newborn
+
Congenital malformations of the urinary system (Q60-Q64)
  
*'''[[P94.9]]''' Disorder of muscle tone of newborn, unspecified
+
*'''[[Q60]]''' Renal agenesis and other reduction defects of kidney
  
*'''[[P95]]''' Stillbirth
+
''Includes''  
  
Deadborn fetus NOS
+
congenital absence of kidney
  
Fetal death of unspecified cause
+
congenital atrophy of kidney
  
Stillbirth NOS
+
infantile atrophy of kidney
  
''Excludes1''  
+
*'''[[Q60.0]]''' Renal agenesis, unilateral
  
maternal care for intrauterine death (O36.4)
+
*'''[[Q60.1]]''' Renal agenesis, bilateral
  
missed abortion (O02.1)
+
*'''[[Q60.2]]''' Renal agenesis, unspecified
  
outcome of delivery, stillbirth (Z37.1, Z37.3, Z37.4, Z37.7)
+
*'''[[Q60.3]]''' Renal hypoplasia, unilateral
  
*'''[[P96]]''' Other conditions originating in the perinatal period
+
*'''[[Q60.4]]''' Renal hypoplasia, bilateral
  
*'''[[P96.0]]''' Congenital renal failure
+
*'''[[Q60.5]]''' Renal hypoplasia, unspecified
  
Uremia of newborn
+
*'''[[Q60.6]]''' Potter's syndrome
  
*'''[[P96.1]]''' Neonatal withdrawal symptoms from maternal use of drugs of addiction
+
*'''[[Q61]]''' Cystic kidney disease
  
Drug withdrawal syndrome in infant of dependent mother
+
''Excludes1''
  
Neonatal abstinence syndrome
+
acquired cyst of kidney (N28.1)
  
''Excludes1''
+
Potter's syndrome (Q60.6)
  
reactions and intoxications from maternal opiates and tranquilizers administered during labor and
+
*'''[[Q61.0]]''' Congenital renal cyst
  
delivery (P04.0)
+
*'''[[Q61.00]]''' Congenital renal cyst, unspecified
  
*'''[[P96.2]]''' Withdrawal symptoms from therapeutic use of drugs in newborn
+
Cyst of kidney NOS (congenital)
  
*'''[[P96.3]]''' Wide cranial sutures of newborn
+
*'''[[Q61.01]]''' Congenital single renal cyst
  
Neonatal craniotabes
+
*'''[[Q61.02]]''' Congenital multiple renal cysts
  
*'''[[P96.5]]''' Complication to newborn due to (fetal) intrauterine procedure
+
*'''[[Q61.1]]''' Polycystic kidney, infantile type
  
''Excludes2''
+
Polycystic kidney, autosomal recessive
  
newborn affected by amniocentesis (P00.6)
+
*'''[[Q61.11]]''' Cystic dilatation of collecting ducts
  
*'''[[P96.8]]''' Other specified conditions originating in the perinatal period
+
*'''[[Q61.19]]''' Other polycystic kidney, infantile type
  
*'''[[P96.81]]''' Exposure to (parental) (environmental) tobacco smoke in the perinatal period
+
*'''[[Q61.2]]''' Polycystic kidney, adult type
  
''Excludes2''
+
Polycystic kidney, autosomal dominant
  
newborn affected by in utero exposure to tobacco (P04.2)
+
*'''[[Q61.3]]''' Polycystic kidney, unspecified
  
exposure to environmental tobacco smoke after the perinatal period (Z77.22)
+
*'''[[Q61.4]]''' Renal dysplasia
  
*'''[[P96.82]]''' Delayed separation of umbilical cord
+
Multicystic dysplastic kidney
  
*'''[[P96.83]]''' Meconium staining
+
Multicystic kidney (development)
 +
 
 +
Multicystic kidney disease
 +
 
 +
Multicystic renal dysplasia
  
 
''Excludes1''  
 
''Excludes1''  
  
meconium aspiration (P24.00, P24.01)  
+
polycystic kidney disease (Q61.11-Q61.3)
 +
 
 +
*'''[[Q61.5]]''' Medullary cystic kidney
 +
 
 +
Nephronopthisis
 +
 
 +
Sponge kidney NOS
 +
 
 +
*'''[[Q61.8]]''' Other cystic kidney diseases
 +
 
 +
Fibrocystic kidney
 +
 
 +
Fibrocystic renal degeneration or disease
 +
 
 +
*'''[[Q61.9]]''' Cystic kidney disease, unspecified
 +
 
 +
Meckel-Gruber syndrome
 +
 
 +
*'''[[Q62]]''' Congenital obstructive defects of renal pelvis and congenital malformations of ureter
 +
 
 +
*'''[[Q62.0]]''' Congenital hydronephrosis
 +
 
 +
*'''[[Q62.1]]''' Congenital occlusion of ureter
 +
 
 +
Atresia and stenosis of ureter
 +
 
 +
*'''[[Q62.10]]''' Congenital occlusion of ureter, unspecified
 +
 
 +
*'''[[Q62.11]]''' Congenital occlusion of ureteropelvic junction
 +
 
 +
*'''[[Q62.12]]''' Congenital occlusion of ureterovesical orifice
 +
 
 +
*'''[[Q62.2]]''' Congenital megaureter
 +
 
 +
Congenital dilatation of ureter
 +
 
 +
*'''[[Q62.3]]''' Other obstructive defects of renal pelvis and ureter
 +
 
 +
*'''[[Q62.31]]''' Congenital ureterocele, orthotopic
 +
 
 +
*'''[[Q62.32]]''' Cecoureterocele
 +
 
 +
Ectopic ureterocele
 +
 
 +
*'''[[Q62.39]]''' Other obstructive defects of renal pelvis and ureter
 +
 
 +
Ureteropelvic junction obstruction NOS
 +
 
 +
*'''[[Q62.4]]''' Agenesis of ureter
 +
 
 +
Congenital absence ureter
 +
 
 +
*'''[[Q62.5]]''' Duplication of ureter
 +
 
 +
Accessory ureter
 +
 
 +
Double ureter
 +
 
 +
*'''[[Q62.6]]''' Malposition of ureter
 +
 
 +
*'''[[Q62.60]]''' Malposition of ureter, unspecified
 +
 
 +
*'''[[Q62.61]]''' Deviation of ureter
 +
 
 +
*'''[[Q62.62]]''' Displacement of ureter
 +
 
 +
*'''[[Q62.63]]''' Anomalous implantation of ureter
 +
 
 +
Ectopia of ureter
 +
 
 +
Ectopic ureter
 +
 
 +
*'''[[Q62.69]]''' Other malposition of ureter
 +
 
 +
*'''[[Q62.7]]''' Congenital vesico-uretero-renal reflux
 +
 
 +
*'''[[Q62.8]]''' Other congenital malformations of ureter
 +
 
 +
Anomaly of ureter NOS
 +
 
 +
*'''[[Q63]]''' Other congenital malformations of kidney
 +
 
 +
''Excludes1''
 +
 
 +
congenital nephrotic syndrome (N04.-)
 +
 
 +
*'''[[Q63.0]]''' Accessory kidney
 +
 
 +
*'''[[Q63.1]]''' Lobulated, fused and horseshoe kidney
 +
 
 +
*'''[[Q63.2]]''' Ectopic kidney
 +
 
 +
Congenital displaced kidney
 +
 
 +
Malrotation of kidney
 +
 
 +
*'''[[Q63.3]]''' Hyperplastic and giant kidney
 +
 
 +
Compensatory hypertrophy of kidney
 +
 
 +
*'''[[Q63.8]]''' Other specified congenital malformations of kidney
 +
 
 +
Congenital renal calculi
 +
 
 +
*'''[[Q63.9]]''' Congenital malformation of kidney, unspecified
 +
 
 +
*'''[[Q64]]''' Other congenital malformations of urinary system
 +
 
 +
*'''[[Q64.0]]''' Epispadias
 +
 
 +
''Excludes1''
 +
 
 +
hypospadias (Q54.-)
 +
 
 +
*'''[[Q64.1]]''' Exstrophy of urinary bladder
 +
 
 +
*'''[[Q64.10]]''' Exstrophy of urinary bladder, unspecified
 +
 
 +
Ectopia vesicae
 +
 
 +
*'''[[Q64.11]]''' Supravesical fissure of urinary bladder
 +
 
 +
*'''[[Q64.12]]''' Cloacal exstrophy of urinary bladder
 +
 
 +
*'''[[Q64.19]]''' Other exstrophy of urinary bladder
 +
 
 +
Extroversion of bladder
 +
 
 +
*'''[[Q64.2]]''' Congenital posterior urethral valves
 +
 
 +
*'''[[Q64.3]]''' Other atresia and stenosis of urethra and bladder neck
 +
 
 +
*'''[[Q64.31]]''' Congenital bladder neck obstruction
 +
 
 +
Congenital obstruction of vesicourethral orifice
 +
 
 +
*'''[[Q64.32]]''' Congenital stricture of urethra
 +
 
 +
*'''[[Q64.33]]''' Congenital stricture of urinary meatus
 +
 
 +
*'''[[Q64.39]]''' Other atresia and stenosis of urethra and bladder neck
 +
 
 +
Atresia and stenosis of urethra and bladder neck NOS
 +
 
 +
*'''[[Q64.4]]''' Malformation of urachus
 +
 
 +
Cyst of urachus
 +
 
 +
Patent urachus
 +
 
 +
Prolapse of urachus
 +
 
 +
*'''[[Q64.5]]''' Congenital absence of bladder and urethra
 +
 
 +
*'''[[Q64.6]]''' Congenital diverticulum of bladder
 +
 
 +
*'''[[Q64.7]]''' Other and unspecified congenital malformations of bladder and urethra
 +
 
 +
''Excludes1''
 +
 
 +
congenital prolapse of bladder (mucosa) (Q79.4)
 +
 
 +
*'''[[Q64.70]]''' Unspecified congenital malformation of bladder and urethra
 +
 
 +
Malformation of bladder or urethra NOS
 +
 
 +
*'''[[Q64.71]]''' Congenital prolapse of urethra
 +
 
 +
*'''[[Q64.72]]''' Congenital prolapse of urinary meatus
 +
 
 +
*'''[[Q64.73]]''' Congenital urethrorectal fistula
 +
 
 +
*'''[[Q64.74]]''' Double urethra
 +
 
 +
*'''[[Q64.75]]''' Double urinary meatus
 +
 
 +
*'''[[Q64.79]]''' Other congenital malformations of bladder and urethra
 +
 
 +
*'''[[Q64.8]]''' Other specified congenital malformations of urinary system
 +
 
 +
*'''[[Q64.9]]''' Congenital malformation of urinary system, unspecified
 +
 
 +
Congenital anomaly NOS of urinary system
 +
 
 +
Congenital deformity NOS of urinary system
 +
 
 +
Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
 +
 
 +
*'''[[Q65]]''' Congenital deformities of hip
 +
 
 +
''Excludes1''
 +
 
 +
clicking hip (R29.4)
 +
 
 +
*'''[[Q65.0]]''' Congenital dislocation of hip, unilateral
 +
 
 +
*'''[[Q65.00]]''' Congenital dislocation of unspecified hip, unilateral
 +
 
 +
*'''[[Q65.01]]''' Congenital dislocation of right hip, unilateral
 +
 
 +
*'''[[Q65.02]]''' Congenital dislocation of left hip, unilateral
 +
 
 +
*'''[[Q65.1]]''' Congenital dislocation of hip, bilateral
 +
 
 +
*'''[[Q65.2]]''' Congenital dislocation of hip, unspecified
 +
 
 +
*'''[[Q65.3]]''' Congenital partial dislocation of hip, unilateral
 +
 
 +
*'''[[Q65.30]]''' Congenital partial dislocation of unspecified hip, unilateral
 +
 
 +
*'''[[Q65.31]]''' Congenital partial dislocation of right hip, unilateral
 +
 
 +
*'''[[Q65.32]]''' Congenital partial dislocation of left hip, unilateral
 +
 
 +
*'''[[Q65.4]]''' Congenital partial dislocation of hip, bilateral
 +
 
 +
*'''[[Q65.5]]''' Congenital partial dislocation of hip, unspecified
 +
 
 +
*'''[[Q65.6]]''' Congenital unstable hip
 +
 
 +
Congenital dislocatable hip
 +
 
 +
*'''[[Q65.8]]''' Other congenital deformities of hip
 +
 
 +
*'''[[Q65.81]]''' Congenital coxa valga
 +
 
 +
*'''[[Q65.82]]''' Congenital coxa vara
 +
 
 +
*'''[[Q65.89]]''' Other specified congenital deformities of hip
 +
 
 +
Anteversion of femoral neck
 +
 
 +
Congenital acetabular dysplasia
 +
 
 +
*'''[[Q65.9]]''' Congenital deformity of hip, unspecified
 +
 
 +
*'''[[Q66]]''' Congenital deformities of feet
 +
 
 +
''Excludes1''
 +
 
 +
reduction defects of feet (Q72.-)
 +
 
 +
valgus deformities (acquired) (M21.0-)
 +
 
 +
varus deformities (acquired) (M21.1-)
 +
 
 +
*'''[[Q66.0]]''' Congenital talipes equinovarus
 +
 
 +
*'''[[Q66.00]]''' Congenital talipes equinovarus, unspecified foot
 +
 
 +
*'''[[Q66.01]]''' Congenital talipes equinovarus, right foot
 +
 
 +
*'''[[Q66.02]]''' Congenital talipes equinovarus, left foot
 +
 
 +
*'''[[Q66.1]]''' Congenital talipes calcaneovarus
 +
 
 +
*'''[[Q66.10]]''' Congenital talipes calcaneovarus, unspecified foot
 +
 
 +
*'''[[Q66.11]]''' Congenital talipes calcaneovarus, right foot
 +
 
 +
*'''[[Q66.12]]''' Congenital talipes calcaneovarus, left foot
 +
 
 +
*'''[[Q66.2]]''' Congenital metatarsus (primus) varus
 +
 
 +
*'''[[Q66.21]]''' Congenital metatarsus primus varus
 +
 
 +
*'''[[Q66.211]]''' Congenital metatarsus primus varus, right foot
 +
 
 +
*'''[[Q66.212]]''' Congenital metatarsus primus varus, left foot
 +
 
 +
*'''[[Q66.219]]''' Congenital metatarsus primus varus, unspecified foot
 +
 
 +
*'''[[Q66.22]]''' Congenital metatarsus adductus
 +
 
 +
Congenital metatarsus varus
 +
 
 +
*'''[[Q66.221]]''' Congenital metatarsus adductus, right foot
 +
 
 +
*'''[[Q66.222]]''' Congenital metatarsus adductus, left foot
 +
 
 +
*'''[[Q66.229]]''' Congenital metatarsus adductus, unspecified foot
 +
 
 +
*'''[[Q66.3]]''' Other congenital varus deformities of feet
 +
 
 +
Hallux varus, congenital
 +
 
 +
*'''[[Q66.30]]''' Other congenital varus deformities of feet, unspecified foot
 +
 
 +
*'''[[Q66.31]]''' Other congenital varus deformities of feet, right foot
 +
 
 +
*'''[[Q66.32]]''' Other congenital varus deformities of feet, left foot
 +
 
 +
*'''[[Q66.4]]''' Congenital talipes calcaneovalgus
 +
 
 +
*'''[[Q66.40]]''' Congenital talipes calcaneovalgus, unspecified foot
 +
 
 +
*'''[[Q66.41]]''' Congenital talipes calcaneovalgus, right foot
 +
 
 +
*'''[[Q66.42]]''' Congenital talipes calcaneovalgus, left foot
 +
 
 +
*'''[[Q66.5]]''' Congenital pes planus
 +
 
 +
Congenital flat foot
 +
 
 +
Congenital rigid flat foot
 +
 
 +
Congenital spastic (everted) flat foot
 +
 
 +
''Excludes1''
 +
 
 +
pes planus, acquired (M21.4)
 +
 
 +
*'''[[Q66.50]]''' Congenital pes planus, unspecified foot
 +
 
 +
*'''[[Q66.51]]''' Congenital pes planus, right foot
 +
 
 +
*'''[[Q66.52]]''' Congenital pes planus, left foot
 +
 
 +
*'''[[Q66.6]]''' Other congenital valgus deformities of feet
 +
 
 +
Congenital metatarsus valgus
 +
 
 +
*'''[[Q66.7]]''' Congenital pes cavus
 +
 
 +
*'''[[Q66.70]]''' Congenital pes cavus, unspecified foot
 +
 
 +
*'''[[Q66.71]]''' Congenital pes cavus, right foot
 +
 
 +
*'''[[Q66.72]]''' Congenital pes cavus, left foot
 +
 
 +
*'''[[Q66.8]]''' Other congenital deformities of feet
 +
 
 +
*'''[[Q66.80]]''' Congenital vertical talus deformity, unspecified foot
 +
 
 +
*'''[[Q66.81]]''' Congenital vertical talus deformity, right foot
 +
 
 +
*'''[[Q66.82]]''' Congenital vertical talus deformity, left foot
 +
 
 +
*'''[[Q66.89]]''' Other specified congenital deformities of feet
 +
 
 +
Congenital asymmetric talipes
 +
 
 +
Congenital clubfoot NOS
 +
 
 +
Congenital talipes NOS
 +
 
 +
Congenital tarsal coalition
 +
 
 +
Hammer toe, congenital
 +
 
 +
*'''[[Q66.9]]''' Congenital deformity of feet, unspecified
 +
 
 +
*'''[[Q66.90]]''' Congenital deformity of feet, unspecified, unspecified foot
 +
 
 +
*'''[[Q66.91]]''' Congenital deformity of feet, unspecified, right foot
 +
 
 +
*'''[[Q66.92]]''' Congenital deformity of feet, unspecified, left foot
 +
 
 +
*'''[[Q67]]''' Congenital musculoskeletal deformities of head, face, spine and chest
 +
 
 +
''Excludes1''
 +
 
 +
congenital malformation syndromes classified to Q87.-
 +
 
 +
Potter's syndrome (Q60.6)
 +
 
 +
*'''[[Q67.0]]''' Congenital facial asymmetry
 +
 
 +
*'''[[Q67.1]]''' Congenital compression facies
 +
 
 +
*'''[[Q67.2]]''' Dolichocephaly
 +
 
 +
*'''[[Q67.3]]''' Plagiocephaly
 +
 
 +
*'''[[Q67.4]]''' Other congenital deformities of skull, face and jaw
 +
 
 +
Congenital depressions in skull
 +
 
 +
Congenital hemifacial atrophy or hypertrophy
 +
 
 +
Deviation of nasal septum, congenital
 +
 
 +
Squashed or bent nose, congenital
 +
 
 +
''Excludes1''
 +
 
 +
dentofacial anomalies (including malocclusion) (M26.-)
 +
 
 +
syphilitic saddle nose (A50.5)
 +
 
 +
*'''[[Q67.5]]''' Congenital deformity of spine
 +
 
 +
Congenital postural scoliosis
 +
 
 +
Congenital scoliosis NOS
 +
 
 +
''Excludes1''
 +
 
 +
infantile idiopathic scoliosis (M41.0)
 +
 
 +
scoliosis due to congenital bony malformation (Q76.3)
 +
 
 +
*'''[[Q67.6]]''' Pectus excavatum
 +
 
 +
Congenital funnel chest
 +
 
 +
*'''[[Q67.7]]''' Pectus carinatum
 +
 
 +
Congenital pigeon chest
 +
 
 +
*'''[[Q67.8]]''' Other congenital deformities of chest
 +
 
 +
Congenital deformity of chest wall NOS
 +
 
 +
*'''[[Q68]]''' Other congenital musculoskeletal deformities
 +
 
 +
''Excludes1''
 +
 
 +
reduction defects of limb(s) (Q71-Q73)
 +
 
 +
''Excludes2''
 +
 
 +
congenital myotonic chondrodystrophy (G71.13)
 +
 
 +
*'''[[Q68.0]]''' Congenital deformity of sternocleidomastoid muscle
 +
 
 +
Congenital contracture of sternocleidomastoid (muscle)
 +
 
 +
Congenital (sternomastoid) torticollis
 +
 
 +
Sternomastoid tumor (congenital)
 +
 
 +
*'''[[Q68.1]]''' Congenital deformity of finger(s) and hand
 +
 
 +
Congenital clubfinger
 +
 
 +
Spade-like hand (congenital)
 +
 
 +
*'''[[Q68.2]]''' Congenital deformity of knee
 +
 
 +
Congenital dislocation of knee
 +
 
 +
Congenital genu recurvatum
 +
 
 +
*'''[[Q68.3]]''' Congenital bowing of femur
 +
 
 +
''Excludes1''
 +
 
 +
anteversion of femur (neck) (Q65.89)
 +
 
 +
*'''[[Q68.4]]''' Congenital bowing of tibia and fibula
 +
 
 +
*'''[[Q68.5]]''' Congenital bowing of long bones of leg, unspecified
 +
 
 +
*'''[[Q68.6]]''' Discoid meniscus
 +
 
 +
*'''[[Q68.8]]''' Other specified congenital musculoskeletal deformities
 +
 
 +
Congenital deformity of clavicle
 +
 
 +
Congenital deformity of elbow
 +
 
 +
Congenital deformity of forearm
 +
 
 +
Congenital deformity of scapula
 +
 
 +
Congenital deformity of wrist
 +
 
 +
Congenital dislocation of elbow
 +
 
 +
Congenital dislocation of shoulder
 +
 
 +
Congenital dislocation of wrist
 +
 
 +
*'''[[Q69]]''' Polydactyly
 +
 
 +
*'''[[Q69.0]]''' Accessory finger(s)
 +
 
 +
*'''[[Q69.1]]''' Accessory thumb(s)
 +
 
 +
*'''[[Q69.2]]''' Accessory toe(s)
 +
 
 +
Accessory hallux
 +
 
 +
*'''[[Q69.9]]''' Polydactyly, unspecified
 +
 
 +
Supernumerary digit(s) NOS
 +
 
 +
*'''[[Q70]]''' Syndactyly
 +
 
 +
*'''[[Q70.0]]''' Fused fingers
 +
 
 +
Complex syndactyly of fingers with synostosis
 +
 
 +
*'''[[Q70.00]]''' Fused fingers, unspecified hand
 +
 
 +
*'''[[Q70.01]]''' Fused fingers, right hand
 +
 
 +
*'''[[Q70.02]]''' Fused fingers, left hand
 +
 
 +
*'''[[Q70.03]]''' Fused fingers, bilateral
 +
 
 +
*'''[[Q70.1]]''' Webbed fingers
 +
 
 +
Simple syndactyly of fingers without synostosis
 +
 
 +
*'''[[Q70.10]]''' Webbed fingers, unspecified hand
 +
 
 +
*'''[[Q70.11]]''' Webbed fingers, right hand
 +
 
 +
*'''[[Q70.12]]''' Webbed fingers, left hand
 +
 
 +
*'''[[Q70.13]]''' Webbed fingers, bilateral
 +
 
 +
*'''[[Q70.2]]''' Fused toes
 +
 
 +
Complex syndactyly of toes with synostosis
 +
 
 +
*'''[[Q70.20]]''' Fused toes, unspecified foot
 +
 
 +
*'''[[Q70.21]]''' Fused toes, right foot
 +
 
 +
*'''[[Q70.22]]''' Fused toes, left foot
 +
 
 +
*'''[[Q70.23]]''' Fused toes, bilateral
 +
 
 +
*'''[[Q70.3]]''' Webbed toes
 +
 
 +
Simple syndactyly of toes without synostosis
 +
 
 +
*'''[[Q70.30]]''' Webbed toes, unspecified foot
 +
 
 +
*'''[[Q70.31]]''' Webbed toes, right foot
 +
 
 +
*'''[[Q70.32]]''' Webbed toes, left foot
 +
 
 +
*'''[[Q70.33]]''' Webbed toes, bilateral
 +
 
 +
*'''[[Q70.4]]''' Polysyndactyly, unspecified
 +
 
 +
''Excludes1''
 +
 
 +
specified syndactyly of hand and feet - code to specified conditions (Q70.0- -Q70.3-)
 +
 
 +
*'''[[Q70.9]]''' Syndactyly, unspecified
 +
 
 +
Symphalangy NOS
 +
 
 +
*'''[[Q71]]''' Reduction defects of upper limb
 +
 
 +
*'''[[Q71.0]]''' Congenital complete absence of upper limb
 +
 
 +
*'''[[Q71.00]]''' Congenital complete absence of unspecified upper limb
 +
 
 +
*'''[[Q71.01]]''' Congenital complete absence of right upper limb
 +
 
 +
*'''[[Q71.02]]''' Congenital complete absence of left upper limb
 +
 
 +
*'''[[Q71.03]]''' Congenital complete absence of upper limb, bilateral
 +
 
 +
*'''[[Q71.1]]''' Congenital absence of upper arm and forearm with hand present
 +
 
 +
*'''[[Q71.10]]''' Congenital absence of unspecified upper arm and forearm with hand present
 +
 
 +
*'''[[Q71.11]]''' Congenital absence of right upper arm and forearm with hand present
 +
 
 +
*'''[[Q71.12]]''' Congenital absence of left upper arm and forearm with hand present
 +
 
 +
*'''[[Q71.13]]''' Congenital absence of upper arm and forearm with hand present, bilateral
 +
 
 +
*'''[[Q71.2]]''' Congenital absence of both forearm and hand
 +
 
 +
*'''[[Q71.20]]''' Congenital absence of both forearm and hand, unspecified upper limb
 +
 
 +
*'''[[Q71.21]]''' Congenital absence of both forearm and hand, right upper limb
 +
 
 +
*'''[[Q71.22]]''' Congenital absence of both forearm and hand, left upper limb
 +
 
 +
*'''[[Q71.23]]''' Congenital absence of both forearm and hand, bilateral
 +
 
 +
*'''[[Q71.3]]''' Congenital absence of hand and finger
 +
 
 +
*'''[[Q71.30]]''' Congenital absence of unspecified hand and finger
 +
 
 +
*'''[[Q71.31]]''' Congenital absence of right hand and finger
 +
 
 +
*'''[[Q71.32]]''' Congenital absence of left hand and finger
 +
 
 +
*'''[[Q71.33]]''' Congenital absence of hand and finger, bilateral
 +
 
 +
*'''[[Q71.4]]''' Longitudinal reduction defect of radius
 +
 
 +
Clubhand (congenital)
 +
 
 +
Radial clubhand
 +
 
 +
*'''[[Q71.40]]''' Longitudinal reduction defect of unspecified radius
 +
 
 +
*'''[[Q71.41]]''' Longitudinal reduction defect of right radius
 +
 
 +
*'''[[Q71.42]]''' Longitudinal reduction defect of left radius
 +
 
 +
*'''[[Q71.43]]''' Longitudinal reduction defect of radius, bilateral
 +
 
 +
*'''[[Q71.5]]''' Longitudinal reduction defect of ulna
 +
 
 +
*'''[[Q71.50]]''' Longitudinal reduction defect of unspecified ulna
 +
 
 +
*'''[[Q71.51]]''' Longitudinal reduction defect of right ulna
 +
 
 +
*'''[[Q71.52]]''' Longitudinal reduction defect of left ulna
 +
 
 +
*'''[[Q71.53]]''' Longitudinal reduction defect of ulna, bilateral
 +
 
 +
*'''[[Q71.6]]''' Lobster-claw hand
 +
 
 +
*'''[[Q71.60]]''' Lobster-claw hand, unspecified hand
 +
 
 +
*'''[[Q71.61]]''' Lobster-claw right hand
 +
 
 +
*'''[[Q71.62]]''' Lobster-claw left hand
 +
 
 +
*'''[[Q71.63]]''' Lobster-claw hand, bilateral
 +
 
 +
*'''[[Q71.8]]''' Other reduction defects of upper limb
 +
 
 +
*'''[[Q71.81]]''' Congenital shortening of upper limb
 +
 
 +
*'''[[Q71.811]]''' Congenital shortening of right upper limb
 +
 
 +
*'''[[Q71.812]]''' Congenital shortening of left upper limb
 +
 
 +
*'''[[Q71.813]]''' Congenital shortening of upper limb, bilateral
 +
 
 +
*'''[[Q71.819]]''' Congenital shortening of unspecified upper limb
 +
 
 +
*'''[[Q71.89]]''' Other reduction defects of upper limb
 +
 
 +
*'''[[Q71.891]]''' Other reduction defects of right upper limb
 +
 
 +
*'''[[Q71.892]]''' Other reduction defects of left upper limb
 +
 
 +
*'''[[Q71.893]]''' Other reduction defects of upper limb, bilateral
 +
 
 +
*'''[[Q71.899]]''' Other reduction defects of unspecified upper limb
 +
 
 +
*'''[[Q71.9]]''' Unspecified reduction defect of upper limb
 +
 
 +
*'''[[Q71.90]]''' Unspecified reduction defect of unspecified upper limb
 +
 
 +
*'''[[Q71.91]]''' Unspecified reduction defect of right upper limb
 +
 
 +
*'''[[Q71.92]]''' Unspecified reduction defect of left upper limb
 +
 
 +
*'''[[Q71.93]]''' Unspecified reduction defect of upper limb, bilateral
 +
 
 +
*'''[[Q72]]''' Reduction defects of lower limb
 +
 
 +
*'''[[Q72.0]]''' Congenital complete absence of lower limb
 +
 
 +
*'''[[Q72.00]]''' Congenital complete absence of unspecified lower limb
 +
 
 +
*'''[[Q72.01]]''' Congenital complete absence of right lower limb
 +
 
 +
*'''[[Q72.02]]''' Congenital complete absence of left lower limb
 +
 
 +
*'''[[Q72.03]]''' Congenital complete absence of lower limb, bilateral
 +
 
 +
*'''[[Q72.1]]''' Congenital absence of thigh and lower leg with foot present
 +
 
 +
*'''[[Q72.10]]''' Congenital absence of unspecified thigh and lower leg with foot present
 +
 
 +
*'''[[Q72.11]]''' Congenital absence of right thigh and lower leg with foot present
 +
 
 +
*'''[[Q72.12]]''' Congenital absence of left thigh and lower leg with foot present
 +
 
 +
*'''[[Q72.13]]''' Congenital absence of thigh and lower leg with foot present, bilateral
 +
 
 +
*'''[[Q72.2]]''' Congenital absence of both lower leg and foot
 +
 
 +
*'''[[Q72.20]]''' Congenital absence of both lower leg and foot, unspecified lower limb
 +
 
 +
*'''[[Q72.21]]''' Congenital absence of both lower leg and foot, right lower limb
 +
 
 +
*'''[[Q72.22]]''' Congenital absence of both lower leg and foot, left lower limb
 +
 
 +
*'''[[Q72.23]]''' Congenital absence of both lower leg and foot, bilateral
 +
 
 +
*'''[[Q72.3]]''' Congenital absence of foot and toe(s)
 +
 
 +
*'''[[Q72.30]]''' Congenital absence of unspecified foot and toe(s)
 +
 
 +
*'''[[Q72.31]]''' Congenital absence of right foot and toe(s)
 +
 
 +
*'''[[Q72.32]]''' Congenital absence of left foot and toe(s)
 +
 
 +
*'''[[Q72.33]]''' Congenital absence of foot and toe(s), bilateral
 +
 
 +
*'''[[Q72.4]]''' Longitudinal reduction defect of femur
 +
 
 +
Proximal femoral focal deficiency
 +
 
 +
*'''[[Q72.40]]''' Longitudinal reduction defect of unspecified femur
 +
 
 +
*'''[[Q72.41]]''' Longitudinal reduction defect of right femur
 +
 
 +
*'''[[Q72.42]]''' Longitudinal reduction defect of left femur
 +
 
 +
*'''[[Q72.43]]''' Longitudinal reduction defect of femur, bilateral
 +
 
 +
*'''[[Q72.5]]''' Longitudinal reduction defect of tibia
 +
 
 +
*'''[[Q72.50]]''' Longitudinal reduction defect of unspecified tibia
 +
 
 +
*'''[[Q72.51]]''' Longitudinal reduction defect of right tibia
 +
 
 +
*'''[[Q72.52]]''' Longitudinal reduction defect of left tibia
 +
 
 +
*'''[[Q72.53]]''' Longitudinal reduction defect of tibia, bilateral
 +
 
 +
*'''[[Q72.6]]''' Longitudinal reduction defect of fibula
 +
 
 +
*'''[[Q72.60]]''' Longitudinal reduction defect of unspecified fibula
 +
 
 +
*'''[[Q72.61]]''' Longitudinal reduction defect of right fibula
 +
 
 +
*'''[[Q72.62]]''' Longitudinal reduction defect of left fibula
 +
 
 +
*'''[[Q72.63]]''' Longitudinal reduction defect of fibula, bilateral
 +
 
 +
*'''[[Q72.7]]''' Split foot
 +
 
 +
*'''[[Q72.70]]''' Split foot, unspecified lower limb
 +
 
 +
*'''[[Q72.71]]''' Split foot, right lower limb
 +
 
 +
*'''[[Q72.72]]''' Split foot, left lower limb
 +
 
 +
*'''[[Q72.73]]''' Split foot, bilateral
 +
 
 +
*'''[[Q72.8]]''' Other reduction defects of lower limb
 +
 
 +
*'''[[Q72.81]]''' Congenital shortening of lower limb
 +
 
 +
*'''[[Q72.811]]''' Congenital shortening of right lower limb
 +
 
 +
*'''[[Q72.812]]''' Congenital shortening of left lower limb
 +
 
 +
*'''[[Q72.813]]''' Congenital shortening of lower limb, bilateral
 +
 
 +
*'''[[Q72.819]]''' Congenital shortening of unspecified lower limb
 +
 
 +
*'''[[Q72.89]]''' Other reduction defects of lower limb
 +
 
 +
*'''[[Q72.891]]''' Other reduction defects of right lower limb
 +
 
 +
*'''[[Q72.892]]''' Other reduction defects of left lower limb
 +
 
 +
*'''[[Q72.893]]''' Other reduction defects of lower limb, bilateral
 +
 
 +
*'''[[Q72.899]]''' Other reduction defects of unspecified lower limb
 +
 
 +
*'''[[Q72.9]]''' Unspecified reduction defect of lower limb
 +
 
 +
*'''[[Q72.90]]''' Unspecified reduction defect of unspecified lower limb
 +
 
 +
*'''[[Q72.91]]''' Unspecified reduction defect of right lower limb
 +
 
 +
*'''[[Q72.92]]''' Unspecified reduction defect of left lower limb
 +
 
 +
*'''[[Q72.93]]''' Unspecified reduction defect of lower limb, bilateral
 +
 
 +
*'''[[Q73]]''' Reduction defects of unspecified limb
 +
 
 +
*'''[[Q73.0]]''' Congenital absence of unspecified limb(s)
 +
 
 +
Amelia NOS
 +
 
 +
*'''[[Q73.1]]''' Phocomelia, unspecified limb(s)
 +
 
 +
Phocomelia NOS
 +
 
 +
*'''[[Q73.8]]''' Other reduction defects of unspecified limb(s)
 +
 
 +
Longitudinal reduction deformity of unspecified limb(s)
 +
 
 +
Ectromelia of limb NOS
 +
 
 +
Hemimelia of limb NOS
 +
 
 +
Reduction defect of limb NOS
 +
 
 +
*'''[[Q74]]''' Other congenital malformations of limb(s)
 +
 
 +
''Excludes1''
 +
 
 +
polydactyly (Q69.-)
 +
 
 +
reduction defect of limb (Q71-Q73)
 +
 
 +
syndactyly (Q70.-)
 +
 
 +
*'''[[Q74.0]]''' Other congenital malformations of upper limb(s), including shoulder girdle
 +
 
 +
Accessory carpal bones
 +
 
 +
Cleidocranial dysostosis
 +
 
 +
Congenital pseudarthrosis of clavicle
 +
 
 +
Macrodactylia (fingers)
 +
 
 +
Madelung's deformity
 +
 
 +
Radioulnar synostosis
 +
 
 +
Sprengel's deformity
 +
 
 +
Triphalangeal thumb
 +
 
 +
*'''[[Q74.1]]''' Congenital malformation of knee
 +
 
 +
Congenital absence of patella
 +
 
 +
Congenital dislocation of patella
 +
 
 +
Congenital genu valgum
 +
 
 +
Congenital genu varum
 +
 
 +
Rudimentary patella
 +
 
 +
''Excludes1''
 +
 
 +
congenital dislocation of knee (Q68.2)
 +
 
 +
congenital genu recurvatum (Q68.2)
 +
 
 +
nail patella syndrome (Q87.2)
 +
 
 +
*'''[[Q74.2]]''' Other congenital malformations of lower limb(s), including pelvic girdle
 +
 
 +
Congenital fusion of sacroiliac joint
 +
 
 +
Congenital malformation of ankle joint
 +
 
 +
Congenital malformation of sacroiliac joint
 +
 
 +
''Excludes1''
 +
 
 +
anteversion of femur (neck) (Q65.89)
 +
 
 +
*'''[[Q74.3]]''' Arthrogryposis multiplex congenita
 +
 
 +
*'''[[Q74.8]]''' Other specified congenital malformations of limb(s)
 +
 
 +
*'''[[Q74.9]]''' Unspecified congenital malformation of limb(s)
 +
 
 +
Congenital anomaly of limb(s) NOS
 +
 
 +
*'''[[Q75]]''' Other congenital malformations of skull and face bones
 +
 
 +
''Excludes1''
 +
 
 +
congenital malformation of face NOS (Q18.-)
 +
 
 +
congenital malformation syndromes classified to Q87.-
 +
 
 +
dentofacial anomalies (including malocclusion) (M26.-)
 +
 
 +
musculoskeletal deformities of head and face (Q67.0-Q67.4)
 +
 
 +
skull defects associated with congenital anomalies of brain such as
 +
 
 +
anencephaly (Q00.0)
 +
 
 +
encephalocele (Q01.-)
 +
 
 +
hydrocephalus (Q03.-)
 +
 
 +
microcephaly (Q02)
 +
 
 +
*'''[[Q75.0]]''' Craniosynostosis
 +
 
 +
Acrocephaly
 +
 
 +
Imperfect fusion of skull
 +
 
 +
Oxycephaly
 +
 
 +
Trigonocephaly
 +
 
 +
*'''[[Q75.1]]''' Craniofacial dysostosis
 +
 
 +
Crouzon's disease
 +
 
 +
*'''[[Q75.2]]''' Hypertelorism
 +
 
 +
*'''[[Q75.3]]''' Macrocephaly
 +
 
 +
*'''[[Q75.4]]''' Mandibulofacial dysostosis
 +
 
 +
Franceschetti syndrome
 +
 
 +
Treacher Collins syndrome
 +
 
 +
*'''[[Q75.5]]''' Oculomandibular dysostosis
 +
 
 +
*'''[[Q75.8]]''' Other specified congenital malformations of skull and face bones
 +
 
 +
Absence of skull bone, congenital
 +
 
 +
Congenital deformity of forehead
 +
 
 +
Platybasia
 +
 
 +
*'''[[Q75.9]]''' Congenital malformation of skull and face bones, unspecified
 +
 
 +
Congenital anomaly of face bones NOS
 +
 
 +
Congenital anomaly of skull NOS
 +
 
 +
*'''[[Q76]]''' Congenital malformations of spine and bony thorax
 +
 
 +
''Excludes1''
 +
 
 +
congenital musculoskeletal deformities of spine and chest (Q67.5-Q67.8)
 +
 
 +
*'''[[Q76.0]]''' Spina bifida occulta
 +
 
 +
''Excludes1''
 +
 
 +
meningocele (spinal) (Q05.-)
 +
 
 +
spina bifida (aperta) (cystica) (Q05.-)
 +
 
 +
*'''[[Q76.1]]''' Klippel-Feil syndrome
 +
 
 +
Cervical fusion syndrome
 +
 
 +
*'''[[Q76.2]]''' Congenital spondylolisthesis
 +
 
 +
Congenital spondylolysis
 +
 
 +
''Excludes1''
 +
 
 +
spondylolisthesis (acquired) (M43.1-)
 +
 
 +
spondylolysis (acquired) (M43.0-)
 +
 
 +
*'''[[Q76.3]]''' Congenital scoliosis due to congenital bony malformation
 +
 
 +
Hemivertebra fusion or failure of segmentation with scoliosis
 +
 
 +
*'''[[Q76.4]]''' Other congenital malformations of spine, not associated with scoliosis
 +
 
 +
*'''[[Q76.41]]''' Congenital kyphosis
 +
 
 +
*'''[[Q76.411]]''' Congenital kyphosis, occipito-atlanto-axial region
 +
 
 +
*'''[[Q76.412]]''' Congenital kyphosis, cervical region
 +
 
 +
*'''[[Q76.413]]''' Congenital kyphosis, cervicothoracic region
 +
 
 +
*'''[[Q76.414]]''' Congenital kyphosis, thoracic region
 +
 
 +
*'''[[Q76.415]]''' Congenital kyphosis, thoracolumbar region
 +
 
 +
*'''[[Q76.419]]''' Congenital kyphosis, unspecified region
 +
 
 +
*'''[[Q76.42]]''' Congenital lordosis
 +
 
 +
*'''[[Q76.425]]''' Congenital lordosis, thoracolumbar region
 +
 
 +
*'''[[Q76.426]]''' Congenital lordosis, lumbar region
 +
 
 +
*'''[[Q76.427]]''' Congenital lordosis, lumbosacral region
 +
 
 +
*'''[[Q76.428]]''' Congenital lordosis, sacral and sacrococcygeal region
 +
 
 +
*'''[[Q76.429]]''' Congenital lordosis, unspecified region
 +
 
 +
*'''[[Q76.49]]''' Other congenital malformations of spine, not associated with scoliosis
 +
 
 +
Congenital absence of vertebra NOS
 +
 
 +
Congenital fusion of spine NOS
 +
 
 +
Congenital malformation of lumbosacral (joint) (region) NOS
 +
 
 +
Congenital malformation of spine NOS
 +
 
 +
Hemivertebra NOS
 +
 
 +
Malformation of spine NOS
 +
 
 +
Platyspondylisis NOS
 +
 
 +
Supernumerary vertebra NOS
 +
 
 +
*'''[[Q76.5]]''' Cervical rib
 +
 
 +
Supernumerary rib in cervical region
 +
 
 +
*'''[[Q76.6]]''' Other congenital malformations of ribs
 +
 
 +
Accessory rib
 +
 
 +
Congenital absence of rib
 +
 
 +
Congenital fusion of ribs
 +
 
 +
Congenital malformation of ribs NOS
 +
 
 +
''Excludes1''
 +
 
 +
short rib syndrome (Q77.2)
 +
 
 +
*'''[[Q76.7]]''' Congenital malformation of sternum
 +
 
 +
Congenital absence of sternum
 +
 
 +
Sternum bifidum
 +
 
 +
*'''[[Q76.8]]''' Other congenital malformations of bony thorax
 +
 
 +
*'''[[Q76.9]]''' Congenital malformation of bony thorax, unspecified
 +
 
 +
*'''[[Q77]]''' Osteochondrodysplasia with defects of growth of tubular bones and spine
 +
 
 +
''Excludes1''
 +
 
 +
mucopolysaccharidosis (E76.0-E76.3)
 +
 
 +
''Excludes2''
 +
 
 +
congenital myotonic chondrodystrophy (G71.13)
 +
 
 +
*'''[[Q77.0]]''' Achondrogenesis
 +
 
 +
Hypochondrogenesis
 +
 
 +
*'''[[Q77.1]]''' Thanatophoric short stature
 +
 
 +
*'''[[Q77.2]]''' Short rib syndrome
 +
 
 +
Asphyxiating thoracic dysplasia (Jeune)
 +
 
 +
*'''[[Q77.3]]''' Chondrodysplasia punctata
 +
 
 +
''Excludes1''
 +
 
 +
Rhizomelic chondrodysplasia punctata (E71.43)
 +
 
 +
*'''[[Q77.4]]''' Achondroplasia
 +
 
 +
Hypochondroplasia
 +
 
 +
Osteosclerosis congenita
 +
 
 +
*'''[[Q77.5]]''' Diastrophic dysplasia
 +
 
 +
*'''[[Q77.6]]''' Chondroectodermal dysplasia
 +
 
 +
Ellis-van Creveld syndrome
 +
 
 +
*'''[[Q77.7]]''' Spondyloepiphyseal dysplasia
 +
 
 +
*'''[[Q77.8]]''' Other osteochondrodysplasia with defects of growth of tubular bones and spine
 +
 
 +
*'''[[Q77.9]]''' Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
 +
 
 +
*'''[[Q78]]''' Other osteochondrodysplasias
 +
 
 +
''Excludes2''
 +
 
 +
congenital myotonic chondrodystrophy (G71.13)
 +
 
 +
*'''[[Q78.0]]''' Osteogenesis imperfecta
 +
 
 +
Fragilitas ossium
 +
 
 +
Osteopsathyrosis
 +
 
 +
*'''[[Q78.1]]''' Polyostotic fibrous dysplasia
 +
 
 +
Albright(-McCune)(-Sternberg) syndrome
 +
 
 +
*'''[[Q78.2]]''' Osteopetrosis
 +
 
 +
Albers-Schönberg syndrome
 +
 
 +
Osteosclerosis NOS
 +
 
 +
*'''[[Q78.3]]''' Progressive diaphyseal dysplasia
 +
 
 +
Camurati-Engelmann syndrome
 +
 
 +
*'''[[Q78.4]]''' Enchondromatosis
 +
 
 +
Maffucci's syndrome
 +
 
 +
Ollier's disease
 +
 
 +
*'''[[Q78.5]]''' Metaphyseal dysplasia
 +
 
 +
Pyle's syndrome
 +
 
 +
*'''[[Q78.6]]''' Multiple congenital exostoses
 +
 
 +
Diaphyseal aclasis
 +
 
 +
*'''[[Q78.8]]''' Other specified osteochondrodysplasias
 +
 
 +
Osteopoikilosis
 +
 
 +
*'''[[Q78.9]]''' Osteochondrodysplasia, unspecified
 +
 
 +
Chondrodystrophy NOS
 +
 
 +
Osteodystrophy NOS
 +
 
 +
*'''[[Q79]]''' Congenital malformations of musculoskeletal system, not elsewhere classified
 +
 
 +
''Excludes2''
 +
 
 +
congenital (sternomastoid) torticollis (Q68.0)
 +
 
 +
*'''[[Q79.0]]''' Congenital diaphragmatic hernia
 +
 
 +
''Excludes1''
 +
 
 +
congenital hiatus hernia (Q40.1)
 +
 
 +
*'''[[Q79.1]]''' Other congenital malformations of diaphragm
 +
 
 +
Absence of diaphragm
 +
 
 +
Congenital malformation of diaphragm NOS
 +
 
 +
Eventration of diaphragm
 +
 
 +
*'''[[Q79.2]]''' Exomphalos
 +
 
 +
Omphalocele
 +
 
 +
''Excludes1''
 +
 
 +
umbilical hernia (K42.-)
 +
 
 +
*'''[[Q79.3]]''' Gastroschisis
 +
 
 +
*'''[[Q79.4]]''' Prune belly syndrome
 +
 
 +
Congenital prolapse of bladder mucosa
 +
 
 +
Eagle-Barrett syndrome
 +
 
 +
*'''[[Q79.5]]''' Other congenital malformations of abdominal wall
 +
 
 +
''Excludes1''
 +
 
 +
umbilical hernia (K42.-)
 +
 
 +
*'''[[Q79.51]]''' Congenital hernia of bladder
 +
 
 +
*'''[[Q79.59]]''' Other congenital malformations of abdominal wall
 +
 
 +
*'''[[Q79.6]]''' Ehlers-Danlos syndromes
 +
 
 +
*'''[[Q79.60]]''' Ehlers-Danlos syndrome, unspecified
 +
 
 +
*'''[[Q79.61]]''' Classical Ehlers-Danlos syndrome
 +
 
 +
Classical EDS (cEDS)
 +
 
 +
*'''[[Q79.62]]''' Hypermobile Ehlers-Danlos syndrome
 +
 
 +
Hypermobile EDS (hEDS)
 +
 
 +
*'''[[Q79.63]]''' Vascular Ehlers-Danlos syndrome
 +
 
 +
Vascular EDS (vEDS)
 +
 
 +
*'''[[Q79.69]]''' Other Ehlers-Danlos syndromes
 +
 
 +
*'''[[Q79.8]]''' Other congenital malformations of musculoskeletal system
 +
 
 +
Absence of muscle
 +
 
 +
Absence of tendon
 +
 
 +
Accessory muscle
 +
 
 +
Amyotrophia congenita
 +
 
 +
Congenital constricting bands
 +
 
 +
Congenital shortening of tendon
 +
 
 +
Poland syndrome
 +
 
 +
*'''[[Q79.9]]''' Congenital malformation of musculoskeletal system, unspecified
 +
 
 +
Congenital anomaly of musculoskeletal system NOS
 +
 
 +
Congenital deformity of musculoskeletal system NOS
 +
 
 +
Other congenital malformations (Q80-Q89)
 +
 
 +
*'''[[Q80]]''' Congenital ichthyosis
 +
 
 +
''Excludes1''
 +
 
 +
Refsum's disease (G60.1)
 +
 
 +
*'''[[Q80.0]]''' Ichthyosis vulgaris
 +
 
 +
*'''[[Q80.1]]''' X-linked ichthyosis
 +
 
 +
*'''[[Q80.2]]''' Lamellar ichthyosis
 +
 
 +
Collodion baby
 +
 
 +
*'''[[Q80.3]]''' Congenital bullous ichthyosiform erythroderma
 +
 
 +
*'''[[Q80.4]]''' Harlequin fetus
 +
 
 +
*'''[[Q80.8]]''' Other congenital ichthyosis
 +
 
 +
*'''[[Q80.9]]''' Congenital ichthyosis, unspecified
 +
 
 +
*'''[[Q81]]''' Epidermolysis bullosa
 +
 
 +
*'''[[Q81.0]]''' Epidermolysis bullosa simplex
 +
 
 +
''Excludes1''
 +
 
 +
Cockayne's syndrome (Q87.19)
 +
 
 +
*'''[[Q81.1]]''' Epidermolysis bullosa letalis
 +
 
 +
Herlitz' syndrome
 +
 
 +
*'''[[Q81.2]]''' Epidermolysis bullosa dystrophica
 +
 
 +
*'''[[Q81.8]]''' Other epidermolysis bullosa
 +
 
 +
*'''[[Q81.9]]''' Epidermolysis bullosa, unspecified
 +
 
 +
*'''[[Q82]]''' Other congenital malformations of skin
 +
 
 +
''Excludes1''
 +
 
 +
acrodermatitis enteropathica (E83.2)
 +
 
 +
congenital erythropoietic porphyria (E80.0)
 +
 
 +
pilonidal cyst or sinus (L05.-)
 +
 
 +
Sturge-Weber (-Dimitri) syndrome (Q85.8)
 +
 
 +
*'''[[Q82.0]]''' Hereditary lymphedema
 +
 
 +
*'''[[Q82.1]]''' Xeroderma pigmentosum
 +
 
 +
*'''[[Q82.2]]''' Congenital cutaneous mastocytosis
 +
 
 +
Congenital diffuse cutaneous mastocytosis
 +
 
 +
Congenital maculopapular cutaneous mastocytosis
 +
 
 +
Congenital urticaria pigmentosa
 +
 
 +
''Excludes1''
 +
 
 +
cutaneous mastocytosis NOS (D47.01)
 +
 
 +
diffuse cutaneous mastocytosis (with onset after newborn period) (D47.01)
 +
 
 +
malignant mastocytosis (C96.2-)
 +
 
 +
systemic mastocytosis (D47.02)
 +
 
 +
urticaria pigmentosa (non-congenital) (with onset after newborn period) (D47.01)
 +
 
 +
*'''[[Q82.3]]''' Incontinentia pigmenti
 +
 
 +
*'''[[Q82.4]]''' Ectodermal dysplasia (anhidrotic)
 +
 
 +
''Excludes1''
 +
 
 +
Ellis-van Creveld syndrome (Q77.6)
 +
 
 +
*'''[[Q82.5]]''' Congenital non-neoplastic nevus
 +
 
 +
Birthmark NOS
 +
 
 +
Flammeus Nevus
 +
 
 +
Portwine Nevus
 +
 
 +
Sanguineous Nevus
 +
 
 +
Strawberry Nevus
 +
 
 +
Vascular Nevus NOS
 +
 
 +
Verrucous Nevus
 +
 
 +
''Excludes2''
 +
 
 +
Café au lait spots (L81.3)
 +
 
 +
lentigo (L81.4)
 +
 
 +
nevus NOS (D22.-)
 +
 
 +
araneus nevus (I78.1)
 +
 
 +
melanocytic nevus (D22.-)
 +
 
 +
pigmented nevus (D22.-)
 +
 
 +
spider nevus (I78.1)
 +
 
 +
stellar nevus (I78.1)
 +
 
 +
*'''[[Q82.6]]''' Congenital sacral dimple
 +
 
 +
Parasacral dimple
 +
 
 +
''Excludes2''
 +
 
 +
pilonidal cyst with abscess (L05.01)
 +
 
 +
pilonidal cyst without abscess (L05.91)
 +
 
 +
*'''[[Q82.8]]''' Other specified congenital malformations of skin
 +
 
 +
Abnormal palmar creases
 +
 
 +
Accessory skin tags
 +
 
 +
Benign familial pemphigus (Hailey-Hailey)
 +
 
 +
Congenital poikiloderma
 +
 
 +
Cutis laxa (hyperelastica)
 +
 
 +
Dermatoglyphic anomalies
 +
 
 +
Inherited keratosis palmaris et plantaris
 +
 
 +
Keratosis follicularis (Darier-White)
 +
 
 +
''Excludes1''
 +
 
 +
Ehlers-Danlos syndrome (Q79.6-)
 +
 
 +
*'''[[Q82.9]]''' Congenital malformation of skin, unspecified
 +
 
 +
*'''[[Q83]]''' Congenital malformations of breast
 +
 
 +
''Excludes2''
 +
 
 +
absence of pectoral muscle (Q79.8)
 +
 
 +
hypoplasia of breast (N64.82)
 +
 
 +
micromastia (N64.82)
 +
 
 +
*'''[[Q83.0]]''' Congenital absence of breast with absent nipple
 +
 
 +
*'''[[Q83.1]]''' Accessory breast
 +
 
 +
Supernumerary breast
 +
 
 +
*'''[[Q83.2]]''' Absent nipple
 +
 
 +
*'''[[Q83.3]]''' Accessory nipple
 +
 
 +
Supernumerary nipple
 +
 
 +
*'''[[Q83.8]]''' Other congenital malformations of breast
 +
 
 +
*'''[[Q83.9]]''' Congenital malformation of breast, unspecified
 +
 
 +
*'''[[Q84]]''' Other congenital malformations of integument
 +
 
 +
*'''[[Q84.0]]''' Congenital alopecia
 +
 
 +
Congenital atrichosis
 +
 
 +
*'''[[Q84.1]]''' Congenital morphological disturbances of hair, not elsewhere classified
 +
 
 +
Beaded hair
 +
 
 +
Monilethrix
 +
 
 +
Pili annulati
 +
 
 +
''Excludes1''
 +
 
 +
Menkes' kinky hair syndrome (E83.0)
 +
 
 +
*'''[[Q84.2]]''' Other congenital malformations of hair
 +
 
 +
Congenital hypertrichosis
 +
 
 +
Congenital malformation of hair NOS
 +
 
 +
Persistent lanugo
 +
 
 +
*'''[[Q84.3]]''' Anonychia
 +
 
 +
''Excludes1''
 +
 
 +
nail patella syndrome (Q87.2)
 +
 
 +
*'''[[Q84.4]]''' Congenital leukonychia
 +
 
 +
*'''[[Q84.5]]''' Enlarged and hypertrophic nails
 +
 
 +
Congenital onychauxis
 +
 
 +
Pachyonychia
 +
 
 +
*'''[[Q84.6]]''' Other congenital malformations of nails
 +
 
 +
Congenital clubnail
 +
 
 +
Congenital koilonychia
 +
 
 +
Congenital malformation of nail NOS
 +
 
 +
*'''[[Q84.8]]''' Other specified congenital malformations of integument
 +
 
 +
Aplasia cutis congenita
 +
 
 +
*'''[[Q84.9]]''' Congenital malformation of integument, unspecified
 +
 
 +
Congenital anomaly of integument NOS
 +
 
 +
Congenital deformity of integument NOS
 +
 
 +
*'''[[Q85]]''' Phakomatoses, not elsewhere classified
 +
 
 +
''Excludes1''
 +
 
 +
ataxia telangiectasia (Louis-Bar) (G11.3)
 +
 
 +
familial dysautonomia (Riley-Day) (G90.1)
 +
 
 +
*'''[[Q85.0]]''' Neurofibromatosis (nonmalignant)
 +
 
 +
*'''[[Q85.00]]''' Neurofibromatosis, unspecified
 +
 
 +
*'''[[Q85.01]]''' Neurofibromatosis, type 1
 +
 
 +
Von Recklinghausen disease
 +
 
 +
*'''[[Q85.02]]''' Neurofibromatosis, type 2
 +
 
 +
Acoustic neurofibromatosis
 +
 
 +
*'''[[Q85.03]]''' Schwannomatosis
 +
 
 +
*'''[[Q85.09]]''' Other neurofibromatosis
 +
 
 +
*'''[[Q85.1]]''' Tuberous sclerosis
 +
 
 +
Bourneville's disease
 +
 
 +
Epiloia
 +
 
 +
*'''[[Q85.8]]''' Other phakomatoses, not elsewhere classified
 +
 
 +
Peutz-Jeghers Syndrome
 +
 
 +
Sturge-Weber(-Dimitri) syndrome
 +
 
 +
von Hippel-Lindau syndrome
 +
 
 +
''Excludes1''
 +
 
 +
Meckel-Gruber syndrome (Q61.9)
 +
 
 +
*'''[[Q85.9]]''' Phakomatosis, unspecified
 +
 
 +
Hamartosis NOS
 +
 
 +
*'''[[Q86]]''' Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
 +
 
 +
''Excludes2''
 +
 
 +
iodine-deficiency-related hypothyroidism (E00-E02)
 +
 
 +
nonteratogenic effects of substances transmitted via placenta or breast milk (P04.-)
 +
 
 +
*'''[[Q86.0]]''' Fetal alcohol syndrome (dysmorphic)
 +
 
 +
*'''[[Q86.1]]''' Fetal hydantoin syndrome
 +
 
 +
Meadow's syndrome
 +
 
 +
*'''[[Q86.2]]''' Dysmorphism due to warfarin
 +
 
 +
*'''[[Q86.8]]''' Other congenital malformation syndromes due to known exogenous causes
 +
 
 +
*'''[[Q87]]''' Other specified congenital malformation syndromes affecting multiple systems ''Use additional''
 +
 
 +
code(s) to identify all associated manifestations
 +
 
 +
*'''[[Q87.0]]''' Congenital malformation syndromes predominantly affecting facial appearance
 +
 
 +
Acrocephalopolysyndactyly
 +
 
 +
Acrocephalosyndactyly (Apert)
 +
 
 +
Cryptophthalmos syndrome
 +
 
 +
Cyclopia
 +
 
 +
Goldenhar syndrome
 +
 
 +
Moebius syndrome
 +
 
 +
Oro-facial-digital syndrome
 +
 
 +
Robin syndrome
 +
 
 +
Whistling face
 +
 
 +
*'''[[Q87.1]]''' Congenital malformation syndromes predominantly associated with short stature
 +
 
 +
''Excludes1''
 +
 
 +
Ellis-van Creveld syndrome (Q77.6)
 +
 
 +
Smith-Lemli-Opitz syndrome (E78.72)
 +
 
 +
*'''[[Q87.11]]''' Prader-Willi syndrome
 +
 
 +
*'''[[Q87.19]]''' Other congenital malformation syndromes predominantly associated with short stature
 +
 
 +
Aarskog syndrome
 +
 
 +
Cockayne syndrome
 +
 
 +
De Lange syndrome
 +
 
 +
Dubowitz syndrome
 +
 
 +
Noonan syndrome
 +
 
 +
Robinow-Silverman-Smith syndrome
 +
 
 +
Russell-Silver syndrome
 +
 
 +
Seckel syndrome
 +
 
 +
*'''[[Q87.2]]''' Congenital malformation syndromes predominantly involving limbs
 +
 
 +
Holt-Oram syndrome
 +
 
 +
Klippel-Trenaunay-Weber syndrome
 +
 
 +
Nail patella syndrome
 +
 
 +
Rubinstein-Taybi syndrome
 +
 
 +
Sirenomelia syndrome
 +
 
 +
Thrombocytopenia with absent radius (TAR) syndrome
 +
 
 +
VATER syndrome
 +
 
 +
*'''[[Q87.3]]''' Congenital malformation syndromes involving early overgrowth
 +
 
 +
Beckwith-Wiedemann syndrome
 +
 
 +
Sotos syndrome
 +
 
 +
Weaver syndrome
 +
 
 +
*'''[[Q87.4]]''' Marfan's syndrome
 +
 
 +
*'''[[Q87.40]]''' Marfan's syndrome, unspecified
 +
 
 +
*'''[[Q87.41]]''' Marfan's syndrome with cardiovascular manifestations
 +
 
 +
*'''[[Q87.410]]''' Marfan's syndrome with aortic dilation
 +
 
 +
*'''[[Q87.418]]''' Marfan's syndrome with other cardiovascular manifestations
 +
 
 +
*'''[[Q87.42]]''' Marfan's syndrome with ocular manifestations
 +
 
 +
*'''[[Q87.43]]''' Marfan's syndrome with skeletal manifestation
 +
 
 +
*'''[[Q87.5]]''' Other congenital malformation syndromes with other skeletal changes
 +
 
 +
*'''[[Q87.8]]''' Other specified congenital malformation syndromes, not elsewhere classified
 +
 
 +
''Excludes1''
 +
 
 +
Zellweger syndrome (E71.510)
 +
 
 +
*'''[[Q87.81]]''' Alport syndrome ''Use additional''
 +
 
 +
code to identify stage of chronic kidney disease (N18.1-N18.6)
 +
 
 +
*'''[[Q87.82]]''' Arterial tortuosity syndrome
 +
 
 +
*'''[[Q87.89]]''' Other specified congenital malformation syndromes, not elsewhere classified
 +
 
 +
Laurence-Moon (-Bardet)-Biedl syndrome
 +
 
 +
*'''[[Q89]]''' Other congenital malformations, not elsewhere classified
 +
 
 +
*'''[[Q89.0]]''' Congenital absence and malformations of spleen
 +
 
 +
''Excludes1''
 +
 
 +
isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
 +
 
 +
*'''[[Q89.01]]''' Asplenia (congenital)
 +
 
 +
*'''[[Q89.09]]''' Congenital malformations of spleen
 +
 
 +
Congenital splenomegaly
 +
 
 +
*'''[[Q89.1]]''' Congenital malformations of adrenal gland
 +
 
 +
''Excludes1''
 +
 
 +
adrenogenital disorders (E25.-)
 +
 
 +
congenital adrenal hyperplasia (E25.0)
 +
 
 +
*'''[[Q89.2]]''' Congenital malformations of other endocrine glands
 +
 
 +
Congenital malformation of parathyroid or thyroid gland
 +
 
 +
Persistent thyroglossal duct
 +
 
 +
Thyroglossal cyst
 +
 
 +
''Excludes1''
 +
 
 +
congenital goiter (E03.0)
 +
 
 +
congenital hypothyroidism (E03.1)
 +
 
 +
*'''[[Q89.3]]''' Situs inversus
 +
 
 +
Dextrocardia with situs inversus
 +
 
 +
Mirror-image atrial arrangement with situs inversus
 +
 
 +
Situs inversus or transversus abdominalis
 +
 
 +
Situs inversus or transversus thoracis
 +
 
 +
Transposition of abdominal viscera
 +
 
 +
Transposition of thoracic viscera
 +
 
 +
''Excludes1''
 +
 
 +
dextrocardia NOS (Q24.0)
 +
 
 +
*'''[[Q89.4]]''' Conjoined twins
 +
 
 +
Craniopagus
 +
 
 +
Dicephaly
 +
 
 +
Pygopagus
 +
 
 +
Thoracopagus
 +
 
 +
*'''[[Q89.7]]''' Multiple congenital malformations, not elsewhere classified
 +
 
 +
Multiple congenital anomalies NOS
 +
 
 +
Multiple congenital deformities NOS
 +
 
 +
''Excludes1''
 +
 
 +
congenital malformation syndromes affecting multiple systems (Q87.-)
 +
 
 +
*'''[[Q89.8]]''' Other specified congenital malformations ''Use additional''
 +
 
 +
code(s) to identify all associated manifestations
 +
 
 +
*'''[[Q89.9]]''' Congenital malformation, unspecified
 +
 
 +
Congenital anomaly NOS
 +
 
 +
Congenital deformity NOS
 +
 
 +
Chromosomal abnormalities, not elsewhere classified (Q90-Q99)
 +
 
 +
''Excludes2''
 +
 
 +
mitochondrial metabolic disorders (E88.4-)
 +
 
 +
*'''[[Q90]]''' Down syndrome ''Use additional''
 +
 
 +
code(s) to identify any associated physical conditions and degree of intellectual disabilities (F70-F79)
 +
 
 +
*'''[[Q90.0]]''' Trisomy 21, nonmosaicism (meiotic nondisjunction)
 +
 
 +
*'''[[Q90.1]]''' Trisomy 21, mosaicism (mitotic nondisjunction)
 +
 
 +
*'''[[Q90.2]]''' Trisomy 21, translocation
 +
 
 +
*'''[[Q90.9]]''' Down syndrome, unspecified
 +
 
 +
Trisomy 21 NOS
 +
 
 +
*'''[[Q91]]''' Trisomy 18 and Trisomy 13
 +
 
 +
*'''[[Q91.0]]''' Trisomy 18, nonmosaicism (meiotic nondisjunction)
 +
 
 +
*'''[[Q91.1]]''' Trisomy 18, mosaicism (mitotic nondisjunction)
 +
 
 +
*'''[[Q91.2]]''' Trisomy 18, translocation
 +
 
 +
*'''[[Q91.3]]''' Trisomy 18, unspecified
 +
 
 +
*'''[[Q91.4]]''' Trisomy 13, nonmosaicism (meiotic nondisjunction)
 +
 
 +
*'''[[Q91.5]]''' Trisomy 13, mosaicism (mitotic nondisjunction)
 +
 
 +
*'''[[Q91.6]]''' Trisomy 13, translocation
 +
 
 +
*'''[[Q91.7]]''' Trisomy 13, unspecified
 +
 
 +
*'''[[Q92]]''' Other trisomies and partial trisomies of the autosomes, not elsewhere classified
 +
 
 +
''Includes''
 +
 
 +
unbalanced translocations and insertions
 +
 
 +
''Excludes1''
 +
 
 +
trisomies of chromosomes 13, 18, 21 (Q90-Q91)
 +
 
 +
*'''[[Q92.0]]''' Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
 +
 
 +
*'''[[Q92.1]]''' Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
 +
 
 +
*'''[[Q92.2]]''' Partial trisomy
 +
 
 +
Less than whole arm duplicated
 +
 
 +
Whole arm or more duplicated
 +
 
 +
''Excludes1''
 +
 
 +
partial trisomy due to unbalanced translocation (Q92.5)
 +
 
 +
*'''[[Q92.5]]''' Duplications with other complex rearrangements
 +
 
 +
Partial trisomy due to unbalanced translocations ''Code also''
 +
 
 +
any associated deletions due to unbalanced translocations, inversions and insertions (Q93.7)
 +
 
 +
*'''[[Q92.6]]''' Marker chromosomes
 +
 
 +
Trisomies due to dicentrics
 +
 
 +
Trisomies due to extra rings
 +
 
 +
Trisomies due to isochromosomes
 +
 
 +
Individual with marker heterochromatin
 +
 
 +
*'''[[Q92.61]]''' Marker chromosomes in normal individual
 +
 
 +
*'''[[Q92.62]]''' Marker chromosomes in abnormal individual
 +
 
 +
*'''[[Q92.7]]''' Triploidy and polyploidy
 +
 
 +
*'''[[Q92.8]]''' Other specified trisomies and partial trisomies of autosomes
 +
 
 +
Duplications identified by fluorescence in situ hybridization (FISH)
 +
 
 +
Duplications identified by in situ hybridization (ISH)
 +
 
 +
Duplications seen only at prometaphase
 +
 
 +
*'''[[Q92.9]]''' Trisomy and partial trisomy of autosomes, unspecified
 +
 
 +
*'''[[Q93]]''' Monosomies and deletions from the autosomes, not elsewhere classified
 +
 
 +
*'''[[Q93.0]]''' Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
 +
 
 +
*'''[[Q93.1]]''' Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
 +
 
 +
*'''[[Q93.2]]''' Chromosome replaced with ring, dicentric or isochromosome
 +
 
 +
*'''[[Q93.3]]''' Deletion of short arm of chromosome 4
 +
 
 +
Wolff-Hirschorn syndrome
 +
 
 +
*'''[[Q93.4]]''' Deletion of short arm of chromosome 5
 +
 
 +
Cri-du-chat syndrome
 +
 
 +
*'''[[Q93.5]]''' Other deletions of part of a chromosome
 +
 
 +
*'''[[Q93.51]]''' Angelman syndrome
 +
 
 +
*'''[[Q93.59]]''' Other deletions of part of a chromosome
 +
 
 +
*'''[[Q93.7]]''' Deletions with other complex rearrangements
 +
 
 +
Deletions due to unbalanced translocations, inversions and insertions ''Code also''
 +
 
 +
any associated duplications due to unbalanced translocations, inversions and insertions (Q92.5)
 +
 
 +
*'''[[Q93.8]]''' Other deletions from the autosomes
 +
 
 +
*'''[[Q93.81]]''' Velo-cardio-facial syndrome
 +
 
 +
Deletion 22q11.2
 +
 
 +
*'''[[Q93.82]]''' Williams syndrome
 +
 
 +
*'''[[Q93.88]]''' Other microdeletions
 +
 
 +
Miller-Dieker syndrome
 +
 
 +
Smith-Magenis syndrome
 +
 
 +
*'''[[Q93.89]]''' Other deletions from the autosomes
 +
 
 +
Deletions identified by fluorescence in situ hybridization (FISH)
 +
 
 +
Deletions identified by in situ hybridization (ISH)
 +
 
 +
Deletions seen only at prometaphase
 +
 
 +
*'''[[Q93.9]]''' Deletion from autosomes, unspecified
 +
 
 +
*'''[[Q95]]''' Balanced rearrangements and structural markers, not elsewhere classified
 +
 
 +
''Includes''
 +
 
 +
Robertsonian and balanced reciprocal translocations and insertions
 +
 
 +
*'''[[Q95.0]]''' Balanced translocation and insertion in normal individual
 +
 
 +
*'''[[Q95.1]]''' Chromosome inversion in normal individual
 +
 
 +
*'''[[Q95.2]]''' Balanced autosomal rearrangement in abnormal individual
 +
 
 +
*'''[[Q95.3]]''' Balanced sex/autosomal rearrangement in abnormal individual
 +
 
 +
*'''[[Q95.5]]''' Individual with autosomal fragile site
 +
 
 +
*'''[[Q95.8]]''' Other balanced rearrangements and structural markers
 +
 
 +
*'''[[Q95.9]]''' Balanced rearrangement and structural marker, unspecified
 +
 
 +
*'''[[Q96]]''' Turner's syndrome
 +
 
 +
''Excludes1''
 +
 
 +
Noonan syndrome (Q87.19)
 +
 
 +
*'''[[Q96.0]]''' Karyotype 45, X
 +
 
 +
*'''[[Q96.1]]''' Karyotype 46, X iso (Xq)
 +
 
 +
Karyotype 46, isochromosome Xq
 +
 
 +
*'''[[Q96.2]]''' Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
 +
 
 +
Karyotype 46, X with abnormal sex chromosome, except isochromosome Xq
 +
 
 +
*'''[[Q96.3]]''' Mosaicism, 45, X/46, XX or XY
 +
 
 +
*'''[[Q96.4]]''' Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
 +
 
 +
*'''[[Q96.8]]''' Other variants of Turner's syndrome
 +
 
 +
*'''[[Q96.9]]''' Turner's syndrome, unspecified
 +
 
 +
*'''[[Q97]]''' Other sex chromosome abnormalities, female phenotype, not elsewhere classified
 +
 
 +
''Excludes1''
 +
 
 +
Turner's syndrome (Q96.-)
 +
 
 +
*'''[[Q97.0]]''' Karyotype 47, XXX
 +
 
 +
*'''[[Q97.1]]''' Female with more than three X chromosomes
 +
 
 +
*'''[[Q97.2]]''' Mosaicism, lines with various numbers of X chromosomes
 +
 
 +
*'''[[Q97.3]]''' Female with 46, XY karyotype
 +
 
 +
*'''[[Q97.8]]''' Other specified sex chromosome abnormalities, female phenotype
 +
 
 +
*'''[[Q97.9]]''' Sex chromosome abnormality, female phenotype, unspecified
 +
 
 +
*'''[[Q98]]''' Other sex chromosome abnormalities, male phenotype, not elsewhere classified
 +
 
 +
*'''[[Q98.0]]''' Klinefelter syndrome karyotype 47, XXY
 +
 
 +
*'''[[Q98.1]]''' Klinefelter syndrome, male with more than two X chromosomes
 +
 
 +
*'''[[Q98.3]]''' Other male with 46, XX karyotype
 +
 
 +
*'''[[Q98.4]]''' Klinefelter syndrome, unspecified
 +
 
 +
*'''[[Q98.5]]''' Karyotype 47, XYY
 +
 
 +
*'''[[Q98.6]]''' Male with structurally abnormal sex chromosome
 +
 
 +
*'''[[Q98.7]]''' Male with sex chromosome mosaicism
 +
 
 +
*'''[[Q98.8]]''' Other specified sex chromosome abnormalities, male phenotype
 +
 
 +
*'''[[Q98.9]]''' Sex chromosome abnormality, male phenotype, unspecified
 +
 
 +
*'''[[Q99]]''' Other chromosome abnormalities, not elsewhere classified
 +
 
 +
*'''[[Q99.0]]''' Chimera 46, XX/46, XY
 +
 
 +
Chimera 46, XX/46, XY true hermaphrodite
 +
 
 +
*'''[[Q99.1]]''' 46, XX true hermaphrodite
 +
 
 +
46, XX with streak gonads
 +
 
 +
46, XY with streak gonads
  
meconium passage during delivery (P03.82)
+
Pure gonadal dysgenesis
  
*'''[[P96.89]]''' Other specified conditions originating in the perinatal period ''Use additional''
+
*'''[[Q99.2]]''' Fragile X chromosome
  
code to specify condition
+
Fragile X syndrome
  
*'''[[P96.9]]''' Condition originating in the perinatal period, unspecified
+
*'''[[Q99.8]]''' Other specified chromosome abnormalities
  
Congenital debility NOS
+
*'''[[Q99.9]]''' Chromosomal abnormality, unspecified

Revision as of 00:30, 13 October 2019

ICD-10-CM-Chapter 17

Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)

Note

Codes from this chapter are not for use on maternal records

Excludes2

inborn errors of metabolism (E70-E88)

This chapter contains the following blocks

Congenital malformations of the nervous system

Congenital malformations of eye, ear, face and neck

Congenital malformations of the circulatory system

Congenital malformations of the respiratory system

Cleft lip and cleft palate

Other congenital malformations of the digestive system

Congenital malformations of genital organs

Congenital malformations of the urinary system

Congenital malformations and deformations of the musculoskeletal system

Other congenital malformations

Chromosomal abnormalities, not elsewhere classified

Congenital malformations of the nervous system (Q00-Q07)

  • Q00 Anencephaly and similar malformations

Acephaly

Acrania

Amyelencephaly

Hemianencephaly

Hemicephaly

  • Q01 Encephalocele

Includes

Arnold-Chiari syndrome, type III

encephalocystocele

encephalomyelocele

hydroencephalocele

hydromeningocele, cranial

meningocele, cerebral

meningoencephalocele

Excludes1

Meckel-Gruber syndrome (Q61.9)

  • Q01.0 Frontal encephalocele
  • Q01.1 Nasofrontal encephalocele
  • Q01.2 Occipital encephalocele
  • Q01.8 Encephalocele of other sites
  • Q01.9 Encephalocele, unspecified
  • Q02 Microcephaly

Includes

hydromicrocephaly

micrencephalon Code first

, if applicable, congenital Zika virus disease

Excludes1

Meckel-Gruber syndrome (Q61.9)

  • Q03 Congenital hydrocephalus

Includes

hydrocephalus in newborn

Excludes1

Arnold-Chiari syndrome, type II (Q07.0-)

acquired hydrocephalus (G91.-)

hydrocephalus due to congenital toxoplasmosis (P37.1)

hydrocephalus with spina bifida (Q05.0-Q05.4)

  • Q03.0 Malformations of aqueduct of Sylvius

Anomaly of aqueduct of Sylvius

Obstruction of aqueduct of Sylvius, congenital

Stenosis of aqueduct of Sylvius

  • Q03.1 Atresia of foramina of Magendie and Luschka

Dandy-Walker syndrome

  • Q03.8 Other congenital hydrocephalus
  • Q03.9 Congenital hydrocephalus, unspecified
  • Q04 Other congenital malformations of brain

Excludes1

cyclopia (Q87.0)

macrocephaly (Q75.3)

  • Q04.0 Congenital malformations of corpus callosum

Agenesis of corpus callosum

  • Q04.3 Other reduction deformities of brain

Absence of part of brain

Agenesis of part of brain

Agyria

Aplasia of part of brain

Hydranencephaly

Hypoplasia of part of brain

Lissencephaly

Microgyria

Pachygyria

Excludes1

congenital malformations of corpus callosum (Q04.0)

  • Q04.4 Septo-optic dysplasia of brain
  • Q04.6 Congenital cerebral cysts

Porencephaly

Schizencephaly

Excludes1

acquired porencephalic cyst (G93.0)

  • Q04.8 Other specified congenital malformations of brain

Arnold-Chiari syndrome, type IV

Macrogyria

  • Q04.9 Congenital malformation of brain, unspecified

Congenital anomaly NOS of brain

Congenital deformity NOS of brain

Congenital disease or lesion NOS of brain

Multiple anomalies NOS of brain, congenital

  • Q05 Spina bifida

Includes

hydromeningocele (spinal)

meningocele (spinal)

meningomyelocele

myelocele

myelomeningocele

rachischisis

spina bifida (aperta)(cystica)

syringomyelocele Use additional code for any associated

paraplegia (paraparesis) (G82.2-)

Excludes1

Arnold-Chiari syndrome, type II (Q07.0-)

spina bifida occulta (Q76.0)

  • Q05.0 Cervical spina bifida with hydrocephalus
  • Q05.1 Thoracic spina bifida with hydrocephalus

Dorsal spina bifida with hydrocephalus

Thoracolumbar spina bifida with hydrocephalus

  • Q05.2 Lumbar spina bifida with hydrocephalus

Lumbosacral spina bifida with hydrocephalus

  • Q05.3 Sacral spina bifida with hydrocephalus
  • Q05.4 Unspecified spina bifida with hydrocephalus
  • Q05.5 Cervical spina bifida without hydrocephalus
  • Q05.6 Thoracic spina bifida without hydrocephalus

Dorsal spina bifida NOS

Thoracolumbar spina bifida NOS

  • Q05.7 Lumbar spina bifida without hydrocephalus

Lumbosacral spina bifida NOS

  • Q05.8 Sacral spina bifida without hydrocephalus
  • Q05.9 Spina bifida, unspecified
  • Q06 Other congenital malformations of spinal cord
  • Q06.1 Hypoplasia and dysplasia of spinal cord

Atelomyelia

Myelatelia

Myelodysplasia of spinal cord

  • Q06.3 Other congenital cauda equina malformations

Hydrorachis

  • Q06.8 Other specified congenital malformations of spinal cord
  • Q06.9 Congenital malformation of spinal cord, unspecified

Congenital anomaly NOS of spinal cord

Congenital deformity NOS of spinal cord

Congenital disease or lesion NOS of spinal cord

  • Q07 Other congenital malformations of nervous system

Excludes2

congenital central alveolar hypoventilation syndrome (G47.35)

familial dysautonomia (Riley-Day) (G90.1)

neurofibromatosis (nonmalignant) (Q85.0-)

  • Q07.0 Arnold-Chiari syndrome

Arnold-Chiari syndrome, type II

Excludes1

Arnold-Chiari syndrome, type III (Q01.-)

Arnold-Chiari syndrome, type IV (Q04.8)

  • Q07.00 Arnold-Chiari syndrome without spina bifida or hydrocephalus
  • Q07.01 Arnold-Chiari syndrome with spina bifida
  • Q07.02 Arnold-Chiari syndrome with hydrocephalus
  • Q07.03 Arnold-Chiari syndrome with spina bifida and hydrocephalus
  • Q07.8 Other specified congenital malformations of nervous system

Agenesis of nerve

Displacement of brachial plexus

Jaw-winking syndrome

Marcus Gunn's syndrome

  • Q07.9 Congenital malformation of nervous system, unspecified

Congenital anomaly NOS of nervous system

Congenital deformity NOS of nervous system

Congenital disease or lesion NOS of nervous system

Congenital malformations of eye, ear, face and neck (Q10-Q18)

Excludes2

cleft lip and cleft palate (Q35-Q37)

congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)

congenital malformation of larynx (Q31.-)

congenital malformation of lip NEC (Q38.0)

congenital malformation of nose (Q30.-)

congenital malformation of parathyroid gland (Q89.2)

congenital malformation of thyroid gland (Q89.2)

  • Q10 Congenital malformations of eyelid, lacrimal apparatus and orbit

Excludes1

cryptophthalmos NOS (Q11.2)

cryptophthalmos syndrome (Q87.0)

  • Q10.1 Congenital ectropion
  • Q10.2 Congenital entropion
  • Q10.3 Other congenital malformations of eyelid

Ablepharon

Blepharophimosis, congenital

Coloboma of eyelid

Congenital absence or agenesis of cilia

Congenital absence or agenesis of eyelid

Congenital accessory eyelid

Congenital accessory eye muscle

Congenital malformation of eyelid NOS

  • Q10.4 Absence and agenesis of lacrimal apparatus

Congenital absence of punctum lacrimale

  • Q10.5 Congenital stenosis and stricture of lacrimal duct
  • Q10.6 Other congenital malformations of lacrimal apparatus

Congenital malformation of lacrimal apparatus NOS

  • Q10.7 Congenital malformation of orbit
  • Q11 Anophthalmos, microphthalmos and macrophthalmos

Anophthalmos NOS

Agenesis of eye

Aplasia of eye

Cryptophthalmos NOS

Dysplasia of eye

Hypoplasia of eye

Rudimentary eye

Excludes1

cryptophthalmos syndrome (Q87.0)

Excludes1

macrophthalmos in congenital glaucoma (Q15.0)

  • Q12 Congenital lens malformations
  • Q12.0 Congenital cataract
  • Q12.1 Congenital displaced lens
  • Q12.8 Other congenital lens malformations

Microphakia

  • Q12.9 Congenital lens malformation, unspecified
  • Q13 Congenital malformations of anterior segment of eye

Coloboma NOS

Aniridia Use additional

code for associated glaucoma (H42)

  • Q13.2 Other congenital malformations of iris

Anisocoria, congenital

Atresia of pupil

Congenital malformation of iris NOS

Corectopia

  • Q13.3 Congenital corneal opacity
  • Q13.4 Other congenital corneal malformations

Congenital malformation of cornea NOS

Microcornea

Peter's anomaly

  • Q13.8 Other congenital malformations of anterior segment of eye
  • Q13.81 Rieger's anomaly Use additional

code for associated glaucoma (H42)

  • Q13.89 Other congenital malformations of anterior segment of eye
  • Q13.9 Congenital malformation of anterior segment of eye, unspecified
  • Q14 Congenital malformations of posterior segment of eye

Excludes2

optic nerve hypoplasia (H47.03-)

  • Q14.0 Congenital malformation of vitreous humor

Congenital vitreous opacity

  • Q14.1 Congenital malformation of retina

Congenital retinal aneurysm

  • Q14.2 Congenital malformation of optic disc

Coloboma of optic disc

  • Q14.3 Congenital malformation of choroid
  • Q14.8 Other congenital malformations of posterior segment of eye

Coloboma of the fundus

  • Q14.9 Congenital malformation of posterior segment of eye, unspecified
  • Q15 Other congenital malformations of eye

Excludes1

congenital nystagmus (H55.01)

ocular albinism (E70.31-)

optic nerve hypoplasia (H47.03-)

retinitis pigmentosa (H35.52)

  • Q15.0 Congenital glaucoma

Axenfeld's anomaly

Buphthalmos

Glaucoma of childhood

Glaucoma of newborn

Hydrophthalmos

Keratoglobus, congenital, with glaucoma

Macrocornea with glaucoma

Macrophthalmos in congenital glaucoma

Megalocornea with glaucoma

  • Q15.8 Other specified congenital malformations of eye
  • Q15.9 Congenital malformation of eye, unspecified

Congenital anomaly of eye

Congenital deformity of eye

  • Q16 Congenital malformations of ear causing impairment of hearing

Excludes1

congenital deafness (H90.-)

  • Q16.0 Congenital absence of (ear) auricle
  • Q16.1 Congenital absence, atresia and stricture of auditory canal (external)

Congenital atresia or stricture of osseous meatus

  • Q16.2 Absence of eustachian tube
  • Q16.3 Congenital malformation of ear ossicles

Congenital fusion of ear ossicles

  • Q16.4 Other congenital malformations of middle ear

Congenital malformation of middle ear NOS

  • Q16.5 Congenital malformation of inner ear

Congenital anomaly of membranous labyrinth

Congenital anomaly of organ of Corti

  • Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified

Congenital absence of ear NOS

  • Q17 Other congenital malformations of ear

Excludes1

congenital malformations of ear with impairment of hearing (Q16.0-Q16.9)

preauricular sinus (Q18.1)

Accessory tragus

Polyotia

Preauricular appendage or tag

Supernumerary ear

Supernumerary lobule

  • Q17.3 Other misshapen ear

Pointed ear

Low-set ears

Excludes1

cervical auricle (Q18.2)

Bat ear

  • Q17.8 Other specified congenital malformations of ear

Congenital absence of lobe of ear

  • Q17.9 Congenital malformation of ear, unspecified

Congenital anomaly of ear NOS

  • Q18 Other congenital malformations of face and neck

Excludes1

cleft lip and cleft palate (Q35-Q37)

conditions classified to Q67.0-Q67.4

congenital malformations of skull and face bones (Q75.-)

cyclopia (Q87.0)

dentofacial anomalies (including malocclusion) (M26.-)

malformation syndromes affecting facial appearance (Q87.0)

persistent thyroglossal duct (Q89.2)

  • Q18.0 Sinus, fistula and cyst of branchial cleft

Branchial vestige

  • Q18.1 Preauricular sinus and cyst

Fistula of auricle, congenital

Cervicoaural fistula

  • Q18.2 Other branchial cleft malformations

Branchial cleft malformation NOS

Cervical auricle

Otocephaly

Pterygium colli

Hypertrophy of lip, congenital

  • Q18.8 Other specified congenital malformations of face and neck

Medial cyst of face and neck

Medial fistula of face and neck

Medial sinus of face and neck

  • Q18.9 Congenital malformation of face and neck, unspecified

Congenital anomaly NOS of face and neck

Congenital malformations of the circulatory system (Q20-Q28)

  • Q20 Congenital malformations of cardiac chambers and connections

Excludes1

dextrocardia with situs inversus (Q89.3)

mirror-image atrial arrangement with situs inversus (Q89.3)

  • Q20.0 Common arterial trunk

Persistent truncus arteriosus

Excludes1

aortic septal defect (Q21.4)

  • Q20.1 Double outlet right ventricle

Taussig-Bing syndrome

  • Q20.2 Double outlet left ventricle
  • Q20.3 Discordant ventriculoarterial connection

Dextrotransposition of aorta

Transposition of great vessels (complete)

  • Q20.4 Double inlet ventricle

Common ventricle

Cor triloculare biatriatum

Single ventricle

  • Q20.5 Discordant atrioventricular connection

Corrected transposition

Levotransposition

Ventricular inversion

  • Q20.6 Isomerism of atrial appendages

Isomerism of atrial appendages with asplenia or polysplenia

  • Q20.8 Other congenital malformations of cardiac chambers and connections

Cor binoculare

  • Q20.9 Congenital malformation of cardiac chambers and connections, unspecified
  • Q21 Congenital malformations of cardiac septa

Excludes1

acquired cardiac septal defect (I51.0)

  • Q21.0 Ventricular septal defect

Roger's disease

  • Q21.1 Atrial septal defect

Coronary sinus defect

Patent or persistent foramen ovale

Patent or persistent ostium secundum defect (type II)

Patent or persistent sinus venosus defect

  • Q21.2 Atrioventricular septal defect

Common atrioventricular canal

Endocardial cushion defect

Ostium primum atrial septal defect (type I)

  • Q21.3 Tetralogy of Fallot

Ventricular septal defect with pulmonary stenosis or atresia, dextroposition of aorta and hypertrophy of right

ventricle

  • Q21.4 Aortopulmonary septal defect

Aortic septal defect

Aortopulmonary window

  • Q21.8 Other congenital malformations of cardiac septa

Eisenmenger's defect

Pentalogy of Fallot Code also

if applicable

Eisenmenger's complex (I27.83)

Eisenmenger's syndrome (I27.83)

  • Q21.9 Congenital malformation of cardiac septum, unspecified

Septal (heart) defect NOS

  • Q22 Congenital malformations of pulmonary and tricuspid valves
  • Q22.0 Pulmonary valve atresia
  • Q22.1 Congenital pulmonary valve stenosis
  • Q22.2 Congenital pulmonary valve insufficiency

Congenital pulmonary valve regurgitation

  • Q22.3 Other congenital malformations of pulmonary valve

Congenital malformation of pulmonary valve NOS

Supernumerary cusps of pulmonary valve

  • Q22.4 Congenital tricuspid stenosis

Congenital tricuspid atresia

  • Q22.6 Hypoplastic right heart syndrome
  • Q22.8 Other congenital malformations of tricuspid valve
  • Q22.9 Congenital malformation of tricuspid valve, unspecified
  • Q23 Congenital malformations of aortic and mitral valves
  • Q23.0 Congenital stenosis of aortic valve

Congenital aortic atresia

Congenital aortic stenosis NOS

Excludes1

congenital stenosis of aortic valve in hypoplastic left heart syndrome (Q23.4)

congenital subaortic stenosis (Q24.4)

supravalvular aortic stenosis (congenital) (Q25.3)

  • Q23.1 Congenital insufficiency of aortic valve

Bicuspid aortic valve

Congenital aortic insufficiency

  • Q23.2 Congenital mitral stenosis

Congenital mitral atresia

  • Q23.3 Congenital mitral insufficiency
  • Q23.4 Hypoplastic left heart syndrome
  • Q23.8 Other congenital malformations of aortic and mitral valves
  • Q23.9 Congenital malformation of aortic and mitral valves, unspecified
  • Q24 Other congenital malformations of heart

Excludes1

endocardial fibroelastosis (I42.4)

Excludes1

dextrocardia with situs inversus (Q89.3)

isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)

mirror-image atrial arrangement with situs inversus (Q89.3)

  • Q24.3 Pulmonary infundibular stenosis

Subvalvular pulmonic stenosis

  • Q24.4 Congenital subaortic stenosis
  • Q24.5 Malformation of coronary vessels

Congenital coronary (artery) aneurysm

  • Q24.6 Congenital heart block
  • Q24.8 Other specified congenital malformations of heart

Congenital diverticulum of left ventricle

Congenital malformation of myocardium

Congenital malformation of pericardium

Malposition of heart

Uhl's disease

  • Q24.9 Congenital malformation of heart, unspecified

Congenital anomaly of heart

Congenital disease of heart

  • Q25 Congenital malformations of great arteries
  • Q25.0 Patent ductus arteriosus

Patent ductus Botallo

Persistent ductus arteriosus

  • Q25.1 Coarctation of aorta

Coarctation of aorta (preductal) (postductal)

Stenosis of aorta

  • Q25.21 Interruption of aortic arch

Atresia of aortic arch

Atresia of aorta

  • Q25.3 Supravalvular aortic stenosis

Excludes1

congenital aortic stenosis NOS (Q23.0)

congenital stenosis of aortic valve (Q23.0)

  • Q25.4 Other congenital malformations of aorta

Excludes1

hypoplasia of aorta in hypoplastic left heart syndrome (Q23.4)

  • Q25.40 Congenital malformation of aorta unspecified
  • Q25.41 Absence and aplasia of aorta
  • Q25.43 Congenital aneurysm of aorta

Congenital aneurysm of aortic root

Congenital aneurysm of aortic sinus

  • Q25.44 Congenital dilation of aorta

Vascular ring of aorta

Persistent convolutions of aortic arch

Persistent right aortic arch

  • Q25.48 Anomalous origin of subclavian artery
  • Q25.49 Other congenital malformations of aorta

Aortic arch

Bovine arch

  • Q25.5 Atresia of pulmonary artery
  • Q25.6 Stenosis of pulmonary artery

Supravalvular pulmonary stenosis

  • Q25.7 Other congenital malformations of pulmonary artery
  • Q25.71 Coarctation of pulmonary artery
  • Q25.72 Congenital pulmonary arteriovenous malformation

Congenital pulmonary arteriovenous aneurysm

  • Q25.79 Other congenital malformations of pulmonary artery

Aberrant pulmonary artery

Agenesis of pulmonary artery

Congenital aneurysm of pulmonary artery

Congenital anomaly of pulmonary artery

Hypoplasia of pulmonary artery

  • Q25.8 Other congenital malformations of other great arteries
  • Q25.9 Congenital malformation of great arteries, unspecified
  • Q26 Congenital malformations of great veins
  • Q26.0 Congenital stenosis of vena cava

Congenital stenosis of vena cava (inferior)(superior)

  • Q26.1 Persistent left superior vena cava
  • Q26.2 Total anomalous pulmonary venous connection

Total anomalous pulmonary venous return (TAPVR), subdiaphragmatic

Total anomalous pulmonary venous return (TAPVR), supradiaphragmatic

  • Q26.3 Partial anomalous pulmonary venous connection

Partial anomalous pulmonary venous return

  • Q26.4 Anomalous pulmonary venous connection, unspecified
  • Q26.5 Anomalous portal venous connection
  • Q26.6 Portal vein-hepatic artery fistula
  • Q26.8 Other congenital malformations of great veins

Absence of vena cava (inferior) (superior)

Azygos continuation of inferior vena cava

Persistent left posterior cardinal vein

Scimitar syndrome

  • Q26.9 Congenital malformation of great vein, unspecified

Congenital anomaly of vena cava (inferior) (superior) NOS

  • Q27 Other congenital malformations of peripheral vascular system

Excludes2

anomalies of cerebral and precerebral vessels (Q28.0-Q28.3)

anomalies of coronary vessels (Q24.5)

anomalies of pulmonary artery (Q25.5-Q25.7)

congenital retinal aneurysm (Q14.1)

hemangioma and lymphangioma (D18.-)

  • Q27.0 Congenital absence and hypoplasia of umbilical artery

Single umbilical artery

  • Q27.1 Congenital renal artery stenosis
  • Q27.2 Other congenital malformations of renal artery

Congenital malformation of renal artery NOS

Multiple renal arteries

  • Q27.3 Arteriovenous malformation (peripheral)

Arteriovenous aneurysm

Excludes1

acquired arteriovenous aneurysm (I77.0)

Excludes2

arteriovenous malformation of cerebral vessels (Q28.2)

arteriovenous malformation of precerebral vessels (Q28.0)

  • Q27.30 Arteriovenous malformation, site unspecified
  • Q27.31 Arteriovenous malformation of vessel of upper limb
  • Q27.32 Arteriovenous malformation of vessel of lower limb
  • Q27.33 Arteriovenous malformation of digestive system vessel
  • Q27.34 Arteriovenous malformation of renal vessel
  • Q27.39 Arteriovenous malformation, other site
  • Q27.4 Congenital phlebectasia
  • Q27.8 Other specified congenital malformations of peripheral vascular system

Absence of peripheral vascular system

Atresia of peripheral vascular system

Congenital aneurysm (peripheral)

Congenital stricture, artery

Congenital varix

Excludes1

arteriovenous malformation (Q27.3-)

  • Q27.9 Congenital malformation of peripheral vascular system, unspecified

Anomaly of artery or vein NOS

  • Q28 Other congenital malformations of circulatory system

Excludes1

congenital aneurysm NOS (Q27.8)

congenital coronary aneurysm (Q24.5)

ruptured cerebral arteriovenous malformation (I60.8)

ruptured malformation of precerebral vessels (I72.0)

Excludes2

congenital peripheral aneurysm (Q27.8)

congenital pulmonary aneurysm (Q25.79)

congenital retinal aneurysm (Q14.1)

  • Q28.0 Arteriovenous malformation of precerebral vessels

Congenital arteriovenous precerebral aneurysm (nonruptured)

  • Q28.1 Other malformations of precerebral vessels

Congenital malformation of precerebral vessels NOS

Congenital precerebral aneurysm (nonruptured)

  • Q28.2 Arteriovenous malformation of cerebral vessels

Arteriovenous malformation of brain NOS

Congenital arteriovenous cerebral aneurysm (nonruptured)

  • Q28.3 Other malformations of cerebral vessels

Congenital cerebral aneurysm (nonruptured)

Congenital malformation of cerebral vessels NOS

Developmental venous anomaly

  • Q28.8 Other specified congenital malformations of circulatory system

Congenital aneurysm, specified site NEC

Spinal vessel anomaly

  • Q28.9 Congenital malformation of circulatory system, unspecified

Congenital malformations of the respiratory system (Q30-Q34)

  • Q30 Congenital malformations of nose

Excludes1

congenital deviation of nasal septum (Q67.4)

Atresia of nares (anterior) (posterior)

Congenital stenosis of nares (anterior) (posterior)

  • Q30.1 Agenesis and underdevelopment of nose

Congenital absent of nose

  • Q30.2 Fissured, notched and cleft nose
  • Q30.3 Congenital perforated nasal septum
  • Q30.8 Other congenital malformations of nose

Accessory nose

Congenital anomaly of nasal sinus wall

  • Q30.9 Congenital malformation of nose, unspecified
  • Q31 Congenital malformations of larynx

Excludes1

congenital laryngeal stridor NOS (P28.89)

Glottic web of larynx

Subglottic web of larynx

Web of larynx NOS

  • Q31.1 Congenital subglottic stenosis
  • Q31.2 Laryngeal hypoplasia
  • Q31.5 Congenital laryngomalacia
  • Q31.8 Other congenital malformations of larynx

Absence of larynx

Agenesis of larynx

Atresia of larynx

Congenital cleft thyroid cartilage

Congenital fissure of epiglottis

Congenital stenosis of larynx NEC

Posterior cleft of cricoid cartilage

  • Q31.9 Congenital malformation of larynx, unspecified
  • Q32 Congenital malformations of trachea and bronchus

Excludes1

congenital bronchiectasis (Q33.4)

  • Q32.0 Congenital tracheomalacia
  • Q32.1 Other congenital malformations of trachea

Atresia of trachea

Congenital anomaly of tracheal cartilage

Congenital dilatation of trachea

Congenital malformation of trachea

Congenital stenosis of trachea

Congenital tracheocele

  • Q32.2 Congenital bronchomalacia
  • Q32.3 Congenital stenosis of bronchus
  • Q32.4 Other congenital malformations of bronchus

Absence of bronchus

Agenesis of bronchus

Atresia of bronchus

Congenital diverticulum of bronchus

Congenital malformation of bronchus NOS

  • Q33 Congenital malformations of lung
  • Q33.0 Congenital cystic lung

Congenital cystic lung disease

Congenital honeycomb lung

Congenital polycystic lung disease

Excludes1

cystic fibrosis (E84.0)

cystic lung disease, acquired or unspecified (J98.4)

  • Q33.1 Accessory lobe of lung

Azygos lobe (fissured), lung

  • Q33.2 Sequestration of lung

Congenital absence of lung (lobe)

  • Q33.4 Congenital bronchiectasis
  • Q33.5 Ectopic tissue in lung
  • Q33.6 Congenital hypoplasia and dysplasia of lung

Excludes1

pulmonary hypoplasia associated with short gestation (P28.0)

  • Q33.8 Other congenital malformations of lung
  • Q33.9 Congenital malformation of lung, unspecified
  • Q34 Other congenital malformations of respiratory system

Excludes2

congenital central alveolar hypoventilation syndrome (G47.35)

  • Q34.1 Congenital cyst of mediastinum
  • Q34.8 Other specified congenital malformations of respiratory system

Atresia of nasopharynx

  • Q34.9 Congenital malformation of respiratory system, unspecified

Congenital absence of respiratory system

Congenital anomaly of respiratory system NOS

Cleft lip and cleft palate (Q35-Q37) Use additional

code to identify associated malformation of the nose (Q30.2)

Excludes1

Robin's syndrome (Q87.0)

  • Q35 Cleft palate

Includes

fissure of palate

palatoschisis

Excludes1

cleft palate with cleft lip (Q37.-)

  • Q35.5 Cleft hard palate with cleft soft palate
  • Q35.9 Cleft palate, unspecified

Cleft palate NOS

Includes

cheiloschisis

congenital fissure of lip

harelip

labium leporinum

Excludes1

cleft lip with cleft palate (Q37.-)

  • Q36.0 Cleft lip, bilateral
  • Q36.9 Cleft lip, unilateral

Cleft lip NOS

  • Q37 Cleft palate with cleft lip

Includes

cheilopalatoschisis

  • Q37.0 Cleft hard palate with bilateral cleft lip
  • Q37.1 Cleft hard palate with unilateral cleft lip

Cleft hard palate with cleft lip NOS

  • Q37.2 Cleft soft palate with bilateral cleft lip
  • Q37.3 Cleft soft palate with unilateral cleft lip

Cleft soft palate with cleft lip NOS

  • Q37.4 Cleft hard and soft palate with bilateral cleft lip
  • Q37.5 Cleft hard and soft palate with unilateral cleft lip

Cleft hard and soft palate with cleft lip NOS

  • Q37.8 Unspecified cleft palate with bilateral cleft lip
  • Q37.9 Unspecified cleft palate with unilateral cleft lip

Cleft palate with cleft lip NOS

Other congenital malformations of the digestive system (Q38-Q45)

  • Q38 Other congenital malformations of tongue, mouth and pharynx

Excludes1

dentofacial anomalies (M26.-)

macrostomia (Q18.4)

microstomia (Q18.5)

  • Q38.0 Congenital malformations of lips, not elsewhere classified

Congenital fistula of lip

Congenital malformation of lip NOS

Van der Woude's syndrome

Excludes1

cleft lip (Q36.-)

cleft lip with cleft palate (Q37.-)

macrocheilia (Q18.6)

microcheilia (Q18.7)

Tongue tie

Congenital hypertrophy of tongue

  • Q38.3 Other congenital malformations of tongue

Aglossia

Bifid tongue

Congenital adhesion of tongue

Congenital fissure of tongue

Congenital malformation of tongue NOS

Double tongue

Hypoglossia

Hypoplasia of tongue

Microglossia

  • Q38.4 Congenital malformations of salivary glands and ducts

Atresia of salivary glands and ducts

Congenital absence of salivary glands and ducts

Congenital accessory salivary glands and ducts

Congenital fistula of salivary gland

  • Q38.5 Congenital malformations of palate, not elsewhere classified

Congenital absence of uvula

Congenital malformation of palate NOS

Congenital high arched palate

Excludes1

cleft palate (Q35.-)

cleft palate with cleft lip (Q37.-)

  • Q38.6 Other congenital malformations of mouth

Congenital malformation of mouth NOS

  • Q38.7 Congenital pharyngeal pouch

Congenital diverticulum of pharynx

Excludes1

pharyngeal pouch syndrome (D82.1)

  • Q38.8 Other congenital malformations of pharynx

Congenital malformation of pharynx NOS

Imperforate pharynx

  • Q39 Congenital malformations of esophagus
  • Q39.0 Atresia of esophagus without fistula

Atresia of esophagus NOS

  • Q39.1 Atresia of esophagus with tracheo-esophageal fistula

Atresia of esophagus with broncho-esophageal fistula

  • Q39.2 Congenital tracheo-esophageal fistula without atresia

Congenital tracheo-esophageal fistula NOS

  • Q39.3 Congenital stenosis and stricture of esophagus
  • Q39.5 Congenital dilatation of esophagus

Congenital cardiospasm

  • Q39.6 Congenital diverticulum of esophagus

Congenital esophageal pouch

  • Q39.8 Other congenital malformations of esophagus

Congenital absence of esophagus

Congenital displacement of esophagus

Congenital duplication of esophagus

  • Q39.9 Congenital malformation of esophagus, unspecified
  • Q40 Other congenital malformations of upper alimentary tract
  • Q40.0 Congenital hypertrophic pyloric stenosis

Congenital or infantile constriction

Congenital or infantile hypertrophy

Congenital or infantile spasm

Congenital or infantile stenosis

Congenital or infantile stricture

  • Q40.1 Congenital hiatus hernia

Congenital displacement of cardia through esophageal hiatus

Excludes1

congenital diaphragmatic hernia (Q79.0)

  • Q40.2 Other specified congenital malformations of stomach

Congenital displacement of stomach

Congenital diverticulum of stomach

Congenital hourglass stomach

Congenital duplication of stomach

Megalogastria

Microgastria

  • Q40.3 Congenital malformation of stomach, unspecified
  • Q40.8 Other specified congenital malformations of upper alimentary tract
  • Q40.9 Congenital malformation of upper alimentary tract, unspecified

Congenital anomaly of upper alimentary tract

Congenital deformity of upper alimentary tract

  • Q41 Congenital absence, atresia and stenosis of small intestine

Includes

congenital obstruction, occlusion or stricture of small intestine or intestine NOS

Excludes1

cystic fibrosis with intestinal manifestation (E84.11)

meconium ileus NOS (without cystic fibrosis) (P76.0)

  • Q41.0 Congenital absence, atresia and stenosis of duodenum
  • Q41.1 Congenital absence, atresia and stenosis of jejunum

Apple peel syndrome

Imperforate jejunum

  • Q41.2 Congenital absence, atresia and stenosis of ileum
  • Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine
  • Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified

Congenital absence, atresia and stenosis of intestine NOS

  • Q42 Congenital absence, atresia and stenosis of large intestine

Includes

congenital obstruction, occlusion and stricture of large intestine

  • Q42.0 Congenital absence, atresia and stenosis of rectum with fistula
  • Q42.1 Congenital absence, atresia and stenosis of rectum without fistula

Imperforate rectum

  • Q42.2 Congenital absence, atresia and stenosis of anus with fistula
  • Q42.3 Congenital absence, atresia and stenosis of anus without fistula

Imperforate anus

  • Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine
  • Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified
  • Q43 Other congenital malformations of intestine
  • Q43.0 Meckel's diverticulum (displaced) (hypertrophic)

Persistent omphalomesenteric duct

Persistent vitelline duct

  • Q43.1 Hirschsprung's disease

Aganglionosis

Congenital (aganglionic) megacolon

  • Q43.2 Other congenital functional disorders of colon

Congenital dilatation of colon

  • Q43.3 Congenital malformations of intestinal fixation

Congenital omental, anomalous adhesions (bands)

Congenital peritoneal adhesions (bands)

Incomplete rotation of cecum and colon

Insufficient rotation of cecum and colon

Jackson's membrane

Malrotation of colon

Rotation failure of cecum and colon

Universal mesentery

  • Q43.4 Duplication of intestine
  • Q43.6 Congenital fistula of rectum and anus

Excludes1

congenital fistula of anus with absence, atresia and stenosis (Q42.2)

congenital fistula of rectum with absence, atresia and stenosis (Q42.0)

congenital rectovaginal fistula (Q52.2)

congenital urethrorectal fistula (Q64.73)

pilonidal fistula or sinus (L05.-)

Cloaca NOS

  • Q43.8 Other specified congenital malformations of intestine

Congenital blind loop syndrome

Congenital diverticulitis, colon

Congenital diverticulum, intestine

Dolichocolon

Megaloappendix

Megaloduodenum

Microcolon

Transposition of appendix

Transposition of colon

Transposition of intestine

  • Q43.9 Congenital malformation of intestine, unspecified
  • Q44 Congenital malformations of gallbladder, bile ducts and liver
  • Q44.0 Agenesis, aplasia and hypoplasia of gallbladder

Congenital absence of gallbladder

  • Q44.1 Other congenital malformations of gallbladder

Congenital malformation of gallbladder NOS

Intrahepatic gallbladder

  • Q44.2 Atresia of bile ducts
  • Q44.3 Congenital stenosis and stricture of bile ducts
  • Q44.5 Other congenital malformations of bile ducts

Accessory hepatic duct

Biliary duct duplication

Congenital malformation of bile duct NOS

Cystic duct duplication

  • Q44.6 Cystic disease of liver

Fibrocystic disease of liver

  • Q44.7 Other congenital malformations of liver

Accessory liver

Alagille's syndrome

Congenital absence of liver

Congenital hepatomegaly

Congenital malformation of liver NOS

  • Q45 Other congenital malformations of digestive system

Excludes2

congenital diaphragmatic hernia (Q79.0)

congenital hiatus hernia (Q40.1)

  • Q45.0 Agenesis, aplasia and hypoplasia of pancreas

Congenital absence of pancreas

  • Q45.2 Congenital pancreatic cyst
  • Q45.3 Other congenital malformations of pancreas and pancreatic duct

Accessory pancreas

Congenital malformation of pancreas or pancreatic duct NOS

Excludes1

congenital diabetes mellitus (E10.-)

cystic fibrosis (E84.0-E84.9)

fibrocystic disease of pancreas (E84.-)

neonatal diabetes mellitus (P70.2)

  • Q45.8 Other specified congenital malformations of digestive system

Absence (complete) (partial) of alimentary tract NOS

Duplication of digestive system

Malposition, congenital of digestive system

  • Q45.9 Congenital malformation of digestive system, unspecified

Congenital anomaly of digestive system

Congenital deformity of digestive system

Congenital malformations of genital organs (Q50-Q56)

Excludes1

androgen insensitivity syndrome (E34.5-)

syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)

  • Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments
  • Q50.0 Congenital absence of ovary

Excludes1

Turner's syndrome (Q96.-)

  • Q50.01 Congenital absence of ovary, unilateral
  • Q50.02 Congenital absence of ovary, bilateral
  • Q50.1 Developmental ovarian cyst
  • Q50.2 Congenital torsion of ovary
  • Q50.3 Other congenital malformations of ovary

46, XX with streak gonads

  • Q50.39 Other congenital malformation of ovary

Congenital malformation of ovary NOS

  • Q50.4 Embryonic cyst of fallopian tube

Fimbrial cyst

  • Q50.5 Embryonic cyst of broad ligament

Epoophoron cyst

Parovarian cyst

  • Q50.6 Other congenital malformations of fallopian tube and broad ligament

Absence of fallopian tube and broad ligament

Accessory fallopian tube and broad ligament

Atresia of fallopian tube and broad ligament

Congenital malformation of fallopian tube or broad ligament NOS

  • Q51 Congenital malformations of uterus and cervix
  • Q51.0 Agenesis and aplasia of uterus

Congenital absence of uterus

  • Q51.1 Doubling of uterus with doubling of cervix and vagina
  • Q51.10 Doubling of uterus with doubling of cervix and vagina without obstruction

Doubling of uterus with doubling of cervix and vagina NOS

  • Q51.11 Doubling of uterus with doubling of cervix and vagina with obstruction
  • Q51.2 Other doubling of uterus

Doubling of uterus NOS

Septate uterus

  • Q51.20 Other doubling of uterus, unspecified

Septate uterus, unspecified

  • Q51.21 Other complete doubling of uterus

Complete septate uterus

  • Q51.22 Other partial doubling of uterus

Partial septate uterus

  • Q51.28 Other doubling of uterus, other specified

Septate uterus, other specified

Bicornate uterus, complete or partial

Unicornate uterus with or without a separate uterine horn

Uterus with only one functioning horn

  • Q51.5 Agenesis and aplasia of cervix

Congenital absence of cervix

  • Q51.6 Embryonic cyst of cervix
  • Q51.7 Congenital fistulae between uterus and digestive and urinary tracts
  • Q51.8 Other congenital malformations of uterus and cervix
  • Q51.81 Other congenital malformations of uterus

Arcuatus uterus

  • Q51.818 Other congenital malformations of uterus

Müllerian anomaly of uterus NEC

  • Q51.82 Other congenital malformations of cervix
  • Q51.828 Other congenital malformations of cervix
  • Q51.9 Congenital malformation of uterus and cervix, unspecified
  • Q52 Other congenital malformations of female genitalia
  • Q52.0 Congenital absence of vagina

Vaginal agenesis, total or partial

Excludes1

doubling of vagina with doubling of uterus and cervix (Q51.1-)

  • Q52.10 Doubling of vagina, unspecified

Septate vagina NOS

  • Q52.11 Transverse vaginal septum
  • Q52.12 Longitudinal vaginal septum
  • Q52.120 Longitudinal vaginal septum, nonobstructing
  • Q52.121 Longitudinal vaginal septum, obstructing, right side
  • Q52.122 Longitudinal vaginal septum, obstructing, left side
  • Q52.123 Longitudinal vaginal septum, microperforate, right side
  • Q52.124 Longitudinal vaginal septum, microperforate, left side
  • Q52.129 Other and unspecified longitudinal vaginal septum
  • Q52.2 Congenital rectovaginal fistula

Excludes1

cloaca (Q43.7)

  • Q52.4 Other congenital malformations of vagina

Canal of Nuck cyst, congenital

Congenital malformation of vagina NOS

Embryonic vaginal cyst

Gartner's duct cyst

  • Q52.6 Congenital malformation of clitoris
  • Q52.7 Other and unspecified congenital malformations of vulva
  • Q52.70 Unspecified congenital malformations of vulva

Congenital malformation of vulva NOS

  • Q52.71 Congenital absence of vulva
  • Q52.79 Other congenital malformations of vulva

Congenital cyst of vulva

  • Q52.8 Other specified congenital malformations of female genitalia
  • Q52.9 Congenital malformation of female genitalia, unspecified
  • Q53 Undescended and ectopic testicle
  • Q53.00 Ectopic testis, unspecified
  • Q53.01 Ectopic testis, unilateral
  • Q53.02 Ectopic testes, bilateral
  • Q53.1 Undescended testicle, unilateral
  • Q53.10 Unspecified undescended testicle, unilateral
  • Q53.11 Abdominal testis, unilateral
  • Q53.111 Unilateral intraabdominal testis
  • Q53.12 Ectopic perineal testis, unilateral
  • Q53.13 Unilateral high scrotal testis
  • Q53.2 Undescended testicle, bilateral
  • Q53.20 Undescended testicle, unspecified, bilateral
  • Q53.21 Abdominal testis, bilateral
  • Q53.211 Bilateral intraabdominal testes
  • Q53.22 Ectopic perineal testis, bilateral
  • Q53.23 Bilateral high scrotal testes
  • Q53.9 Undescended testicle, unspecified

Cryptorchism NOS

  • Q54 Hypospadias

Excludes1

epispadias (Q64.0)

  • Q54.0 Hypospadias, balanic

Hypospadias, coronal

Hypospadias, glandular

  • Q54.1 Hypospadias, penile
  • Q54.2 Hypospadias, penoscrotal
  • Q54.3 Hypospadias, perineal

Chordee without hypospadias

Hypospadias with intersex state

  • Q54.9 Hypospadias, unspecified
  • Q55 Other congenital malformations of male genital organs

Excludes1

congenital hydrocele (P83.5)

hypospadias (Q54.-)

  • Q55.0 Absence and aplasia of testis

Monorchism

  • Q55.1 Hypoplasia of testis and scrotum

Fusion of testes

  • Q55.2 Other and unspecified congenital malformations of testis and scrotum
  • Q55.20 Unspecified congenital malformations of testis and scrotum

Congenital malformation of testis or scrotum NOS

  • Q55.29 Other congenital malformations of testis and scrotum
  • Q55.3 Atresia of vas deferens Code first

any associated cystic fibrosis (E84.-)

  • Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate

Absence or aplasia of prostate

Absence or aplasia of spermatic cord

Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS

  • Q55.5 Congenital absence and aplasia of penis
  • Q55.6 Other congenital malformations of penis
  • Q55.61 Curvature of penis (lateral)

Micropenis

  • Q55.63 Congenital torsion of penis

Excludes1

acquired torsion of penis (N48.82)

Buried penis

Concealed penis

Excludes1

acquired buried penis (N48.83)

  • Q55.69 Other congenital malformation of penis

Congenital malformation of penis NOS

  • Q55.7 Congenital vasocutaneous fistula
  • Q55.8 Other specified congenital malformations of male genital organs
  • Q55.9 Congenital malformation of male genital organ, unspecified

Congenital anomaly of male genital organ

Congenital deformity of male genital organ

  • Q56 Indeterminate sex and pseudohermaphroditism

Excludes1

46,XX true hermaphrodite (Q99.1)

androgen insensitivity syndrome (E34.5-)

chimera 46,XX/46,XY true hermaphrodite (Q99.0)

female pseudohermaphroditism with adrenocortical disorder (E25.-)

pseudohermaphroditism with specified chromosomal anomaly (Q96-Q99)

pure gonadal dysgenesis (Q99.1)

  • Q56.0 Hermaphroditism, not elsewhere classified

Ovotestis

  • Q56.1 Male pseudohermaphroditism, not elsewhere classified

46, XY with streak gonads

Male pseudohermaphroditism NOS

  • Q56.2 Female pseudohermaphroditism, not elsewhere classified

Female pseudohermaphroditism NOS

  • Q56.3 Pseudohermaphroditism, unspecified
  • Q56.4 Indeterminate sex, unspecified

Ambiguous genitalia

Congenital malformations of the urinary system (Q60-Q64)

  • Q60 Renal agenesis and other reduction defects of kidney

Includes

congenital absence of kidney

congenital atrophy of kidney

infantile atrophy of kidney

  • Q60.0 Renal agenesis, unilateral
  • Q60.1 Renal agenesis, bilateral
  • Q60.2 Renal agenesis, unspecified
  • Q60.3 Renal hypoplasia, unilateral
  • Q60.4 Renal hypoplasia, bilateral
  • Q60.5 Renal hypoplasia, unspecified
  • Q61 Cystic kidney disease

Excludes1

acquired cyst of kidney (N28.1)

Potter's syndrome (Q60.6)

  • Q61.0 Congenital renal cyst
  • Q61.00 Congenital renal cyst, unspecified

Cyst of kidney NOS (congenital)

  • Q61.01 Congenital single renal cyst
  • Q61.02 Congenital multiple renal cysts
  • Q61.1 Polycystic kidney, infantile type

Polycystic kidney, autosomal recessive

  • Q61.11 Cystic dilatation of collecting ducts
  • Q61.19 Other polycystic kidney, infantile type
  • Q61.2 Polycystic kidney, adult type

Polycystic kidney, autosomal dominant

  • Q61.3 Polycystic kidney, unspecified

Multicystic dysplastic kidney

Multicystic kidney (development)

Multicystic kidney disease

Multicystic renal dysplasia

Excludes1

polycystic kidney disease (Q61.11-Q61.3)

  • Q61.5 Medullary cystic kidney

Nephronopthisis

Sponge kidney NOS

  • Q61.8 Other cystic kidney diseases

Fibrocystic kidney

Fibrocystic renal degeneration or disease

  • Q61.9 Cystic kidney disease, unspecified

Meckel-Gruber syndrome

  • Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
  • Q62.0 Congenital hydronephrosis
  • Q62.1 Congenital occlusion of ureter

Atresia and stenosis of ureter

  • Q62.10 Congenital occlusion of ureter, unspecified
  • Q62.11 Congenital occlusion of ureteropelvic junction
  • Q62.12 Congenital occlusion of ureterovesical orifice
  • Q62.2 Congenital megaureter

Congenital dilatation of ureter

  • Q62.3 Other obstructive defects of renal pelvis and ureter
  • Q62.31 Congenital ureterocele, orthotopic

Ectopic ureterocele

  • Q62.39 Other obstructive defects of renal pelvis and ureter

Ureteropelvic junction obstruction NOS

Congenital absence ureter

  • Q62.5 Duplication of ureter

Accessory ureter

Double ureter

  • Q62.6 Malposition of ureter
  • Q62.60 Malposition of ureter, unspecified
  • Q62.63 Anomalous implantation of ureter

Ectopia of ureter

Ectopic ureter

  • Q62.69 Other malposition of ureter
  • Q62.7 Congenital vesico-uretero-renal reflux
  • Q62.8 Other congenital malformations of ureter

Anomaly of ureter NOS

  • Q63 Other congenital malformations of kidney

Excludes1

congenital nephrotic syndrome (N04.-)

  • Q63.1 Lobulated, fused and horseshoe kidney

Congenital displaced kidney

Malrotation of kidney

  • Q63.3 Hyperplastic and giant kidney

Compensatory hypertrophy of kidney

  • Q63.8 Other specified congenital malformations of kidney

Congenital renal calculi

  • Q63.9 Congenital malformation of kidney, unspecified
  • Q64 Other congenital malformations of urinary system

Excludes1

hypospadias (Q54.-)

  • Q64.1 Exstrophy of urinary bladder
  • Q64.10 Exstrophy of urinary bladder, unspecified

Ectopia vesicae

  • Q64.11 Supravesical fissure of urinary bladder
  • Q64.12 Cloacal exstrophy of urinary bladder
  • Q64.19 Other exstrophy of urinary bladder

Extroversion of bladder

  • Q64.2 Congenital posterior urethral valves
  • Q64.3 Other atresia and stenosis of urethra and bladder neck
  • Q64.31 Congenital bladder neck obstruction

Congenital obstruction of vesicourethral orifice

  • Q64.32 Congenital stricture of urethra
  • Q64.33 Congenital stricture of urinary meatus
  • Q64.39 Other atresia and stenosis of urethra and bladder neck

Atresia and stenosis of urethra and bladder neck NOS

  • Q64.4 Malformation of urachus

Cyst of urachus

Patent urachus

Prolapse of urachus

  • Q64.5 Congenital absence of bladder and urethra
  • Q64.6 Congenital diverticulum of bladder
  • Q64.7 Other and unspecified congenital malformations of bladder and urethra

Excludes1

congenital prolapse of bladder (mucosa) (Q79.4)

  • Q64.70 Unspecified congenital malformation of bladder and urethra

Malformation of bladder or urethra NOS

  • Q64.71 Congenital prolapse of urethra
  • Q64.72 Congenital prolapse of urinary meatus
  • Q64.73 Congenital urethrorectal fistula
  • Q64.79 Other congenital malformations of bladder and urethra
  • Q64.8 Other specified congenital malformations of urinary system
  • Q64.9 Congenital malformation of urinary system, unspecified

Congenital anomaly NOS of urinary system

Congenital deformity NOS of urinary system

Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)

  • Q65 Congenital deformities of hip

Excludes1

clicking hip (R29.4)

  • Q65.0 Congenital dislocation of hip, unilateral
  • Q65.00 Congenital dislocation of unspecified hip, unilateral
  • Q65.01 Congenital dislocation of right hip, unilateral
  • Q65.02 Congenital dislocation of left hip, unilateral
  • Q65.1 Congenital dislocation of hip, bilateral
  • Q65.2 Congenital dislocation of hip, unspecified
  • Q65.3 Congenital partial dislocation of hip, unilateral
  • Q65.30 Congenital partial dislocation of unspecified hip, unilateral
  • Q65.31 Congenital partial dislocation of right hip, unilateral
  • Q65.32 Congenital partial dislocation of left hip, unilateral
  • Q65.4 Congenital partial dislocation of hip, bilateral
  • Q65.5 Congenital partial dislocation of hip, unspecified
  • Q65.6 Congenital unstable hip

Congenital dislocatable hip

  • Q65.8 Other congenital deformities of hip
  • Q65.89 Other specified congenital deformities of hip

Anteversion of femoral neck

Congenital acetabular dysplasia

  • Q65.9 Congenital deformity of hip, unspecified
  • Q66 Congenital deformities of feet

Excludes1

reduction defects of feet (Q72.-)

valgus deformities (acquired) (M21.0-)

varus deformities (acquired) (M21.1-)

  • Q66.0 Congenital talipes equinovarus
  • Q66.00 Congenital talipes equinovarus, unspecified foot
  • Q66.01 Congenital talipes equinovarus, right foot
  • Q66.02 Congenital talipes equinovarus, left foot
  • Q66.1 Congenital talipes calcaneovarus
  • Q66.10 Congenital talipes calcaneovarus, unspecified foot
  • Q66.11 Congenital talipes calcaneovarus, right foot
  • Q66.12 Congenital talipes calcaneovarus, left foot
  • Q66.2 Congenital metatarsus (primus) varus
  • Q66.21 Congenital metatarsus primus varus
  • Q66.211 Congenital metatarsus primus varus, right foot
  • Q66.212 Congenital metatarsus primus varus, left foot
  • Q66.219 Congenital metatarsus primus varus, unspecified foot
  • Q66.22 Congenital metatarsus adductus

Congenital metatarsus varus

  • Q66.221 Congenital metatarsus adductus, right foot
  • Q66.222 Congenital metatarsus adductus, left foot
  • Q66.229 Congenital metatarsus adductus, unspecified foot
  • Q66.3 Other congenital varus deformities of feet

Hallux varus, congenital

  • Q66.30 Other congenital varus deformities of feet, unspecified foot
  • Q66.31 Other congenital varus deformities of feet, right foot
  • Q66.32 Other congenital varus deformities of feet, left foot
  • Q66.4 Congenital talipes calcaneovalgus
  • Q66.40 Congenital talipes calcaneovalgus, unspecified foot
  • Q66.41 Congenital talipes calcaneovalgus, right foot
  • Q66.42 Congenital talipes calcaneovalgus, left foot
  • Q66.5 Congenital pes planus

Congenital flat foot

Congenital rigid flat foot

Congenital spastic (everted) flat foot

Excludes1

pes planus, acquired (M21.4)

  • Q66.50 Congenital pes planus, unspecified foot
  • Q66.51 Congenital pes planus, right foot
  • Q66.52 Congenital pes planus, left foot
  • Q66.6 Other congenital valgus deformities of feet

Congenital metatarsus valgus

  • Q66.7 Congenital pes cavus
  • Q66.70 Congenital pes cavus, unspecified foot
  • Q66.71 Congenital pes cavus, right foot
  • Q66.72 Congenital pes cavus, left foot
  • Q66.8 Other congenital deformities of feet
  • Q66.80 Congenital vertical talus deformity, unspecified foot
  • Q66.81 Congenital vertical talus deformity, right foot
  • Q66.82 Congenital vertical talus deformity, left foot
  • Q66.89 Other specified congenital deformities of feet

Congenital asymmetric talipes

Congenital clubfoot NOS

Congenital talipes NOS

Congenital tarsal coalition

Hammer toe, congenital

  • Q66.9 Congenital deformity of feet, unspecified
  • Q66.90 Congenital deformity of feet, unspecified, unspecified foot
  • Q66.91 Congenital deformity of feet, unspecified, right foot
  • Q66.92 Congenital deformity of feet, unspecified, left foot
  • Q67 Congenital musculoskeletal deformities of head, face, spine and chest

Excludes1

congenital malformation syndromes classified to Q87.-

Potter's syndrome (Q60.6)

  • Q67.0 Congenital facial asymmetry
  • Q67.1 Congenital compression facies
  • Q67.4 Other congenital deformities of skull, face and jaw

Congenital depressions in skull

Congenital hemifacial atrophy or hypertrophy

Deviation of nasal septum, congenital

Squashed or bent nose, congenital

Excludes1

dentofacial anomalies (including malocclusion) (M26.-)

syphilitic saddle nose (A50.5)

  • Q67.5 Congenital deformity of spine

Congenital postural scoliosis

Congenital scoliosis NOS

Excludes1

infantile idiopathic scoliosis (M41.0)

scoliosis due to congenital bony malformation (Q76.3)

Congenital funnel chest

Congenital pigeon chest

  • Q67.8 Other congenital deformities of chest

Congenital deformity of chest wall NOS

  • Q68 Other congenital musculoskeletal deformities

Excludes1

reduction defects of limb(s) (Q71-Q73)

Excludes2

congenital myotonic chondrodystrophy (G71.13)

  • Q68.0 Congenital deformity of sternocleidomastoid muscle

Congenital contracture of sternocleidomastoid (muscle)

Congenital (sternomastoid) torticollis

Sternomastoid tumor (congenital)

  • Q68.1 Congenital deformity of finger(s) and hand

Congenital clubfinger

Spade-like hand (congenital)

  • Q68.2 Congenital deformity of knee

Congenital dislocation of knee

Congenital genu recurvatum

  • Q68.3 Congenital bowing of femur

Excludes1

anteversion of femur (neck) (Q65.89)

  • Q68.4 Congenital bowing of tibia and fibula
  • Q68.5 Congenital bowing of long bones of leg, unspecified
  • Q68.8 Other specified congenital musculoskeletal deformities

Congenital deformity of clavicle

Congenital deformity of elbow

Congenital deformity of forearm

Congenital deformity of scapula

Congenital deformity of wrist

Congenital dislocation of elbow

Congenital dislocation of shoulder

Congenital dislocation of wrist

  • Q69 Polydactyly
  • Q69.0 Accessory finger(s)

Accessory hallux

  • Q69.9 Polydactyly, unspecified

Supernumerary digit(s) NOS

Complex syndactyly of fingers with synostosis

  • Q70.00 Fused fingers, unspecified hand
  • Q70.01 Fused fingers, right hand