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 +
ICD-10-CM-Chapter 18
  
ICD-10-CM-Chapter 17
+
Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R99)
  
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
+
Note
  
Note
+
This chapter includes symptoms, signs, abnormal results of clinical or other investigative procedures, and ill-defined
 +
 
 +
conditions regarding which no diagnosis classifiable elsewhere is recorded
  
Codes from this chapter are not for use on maternal records
+
Signs and symptoms that point rather definitely to a given diagnosis have been assigned to a category in other
  
''Excludes2''
+
chapters of the classification. In general, categories in this chapter include the less well-defined conditions and
  
inborn errors of metabolism (E70-E88)
+
symptoms that, without the necessary study of the case to establish a final diagnosis, point perhaps equally to
  
This chapter contains the following blocks
+
two or more diseases or to two or more systems of the body. Practically all categories in the chapter could be
  
*'''[[Q00-Q07]]'''
+
designated 'not otherwise specified', 'unknown etiology' or 'transient'. The Alphabetical Index should be
  
Congenital malformations of the nervous system
+
consulted to determine which symptoms and signs are to be allocated here and which to other chapters. The
  
*'''[[Q10-Q18]]'''
+
residual subcategories, numbered .8, are generally provided for other relevant symptoms that cannot be
  
Congenital malformations of eye, ear, face and neck
+
allocated elsewhere in the classification
  
*'''[[Q20-Q28]]'''
+
The conditions and signs or symptoms included in categories R00-R94 consist of
  
Congenital malformations of the circulatory system
+
(a) cases for which no more specific diagnosis can be made even after all the facts bearing on the case have been
  
*'''[[Q30-Q34]]'''
+
investigated;
  
Congenital malformations of the respiratory system
+
(b) signs or symptoms existing at the time of initial encounter that proved to be transient and whose causes could
  
*'''[[Q35-Q37]]'''
+
not be determined;
  
Cleft lip and cleft palate
+
(c) provisional diagnosis in a patient who failed to return for further investigation or care;
  
*'''[[Q38-Q45]]'''
+
(d) cases referred elsewhere for investigation or treatment before the diagnosis was made;
  
Other congenital malformations of the digestive system
+
(e) cases in which a more precise diagnosis was not available for any other reason;
  
*'''[[Q50-Q56]]'''
+
(f) certain symptoms, for which supplementary information is provided, that represent important problems in medical
  
Congenital malformations of genital organs
+
care in their own right
  
*'''[[Q60-Q64]]'''
+
''Excludes2''  
  
Congenital malformations of the urinary system
+
abnormal findings on antenatal screening of mother (O28.-)
  
*'''[[Q65-Q79]]'''
+
certain conditions originating in the perinatal period (P04-P96)
  
Congenital malformations and deformations of the musculoskeletal system
+
signs and symptoms classified in the body system chapters
  
*'''[[Q80-Q89]]'''
+
signs and symptoms of breast (N63, N64.5)
  
Other congenital malformations
+
This chapter contains the following blocks
  
*'''[[Q90-Q99]]'''
+
*'''[[R00-R09]]'''
  
Chromosomal abnormalities, not elsewhere classified
+
Symptoms and signs involving the circulatory and respiratory systems
  
Congenital malformations of the nervous system (Q00-Q07)
+
*'''[[R10-R19]]'''
  
*'''[[Q00]]''' Anencephaly and similar malformations
+
Symptoms and signs involving the digestive system and abdomen
  
*'''[[Q00.0]]''' Anencephaly
+
*'''[[R20-R23]]'''
  
Acephaly
+
Symptoms and signs involving the skin and subcutaneous tissue
  
Acrania
+
*'''[[R25-R29]]'''
  
Amyelencephaly
+
Symptoms and signs involving the nervous and musculoskeletal systems
  
Hemianencephaly
+
*'''[[R30-R39]]'''
  
Hemicephaly
+
Symptoms and signs involving the genitourinary system
  
*'''[[Q00.1]]''' Craniorachischisis
+
*'''[[R40-R46]]'''
  
*'''[[Q00.2]]''' Iniencephaly
+
Symptoms and signs involving cognition, perception, emotional state and behavior
  
*'''[[Q01]]''' Encephalocele
+
*'''[[R47-R49]]'''
  
''Includes''
+
Symptoms and signs involving speech and voice
  
Arnold-Chiari syndrome, type III
+
*'''[[R50-R69]]'''
  
encephalocystocele
+
General symptoms and signs
  
encephalomyelocele
+
*'''[[R70-R79]]'''
  
hydroencephalocele
+
Abnormal findings on examination of blood, without diagnosis
  
hydromeningocele, cranial
+
*'''[[R80-R82]]'''
  
meningocele, cerebral
+
Abnormal findings on examination of urine, without diagnosis
  
meningoencephalocele
+
*'''[[R83-R89]]'''
  
''Excludes1''
+
Abnormal findings on examination of other body fluids, substances and tissues, without diagnosis
  
Meckel-Gruber syndrome (Q61.9)
+
*'''[[R90-R94]]'''
  
*'''[[Q01.0]]''' Frontal encephalocele
+
Abnormal findings on diagnostic imaging and in function studies, without diagnosis
  
*'''[[Q01.1]]''' Nasofrontal encephalocele
+
*'''[[R97]]'''
  
*'''[[Q01.2]]''' Occipital encephalocele
+
Abnormal tumor markers
  
*'''[[Q01.8]]''' Encephalocele of other sites
+
*'''[[R99]]'''
  
*'''[[Q01.9]]''' Encephalocele, unspecified
+
Ill-defined and unknown cause of mortality
  
*'''[[Q02]]''' Microcephaly
+
Symptoms and signs involving the circulatory and respiratory systems (R00-R09)
  
''Includes''  
+
*'''[[R00]]''' Abnormalities of heart beat
  
hydromicrocephaly
+
''Excludes1''
  
micrencephalon ''Code first''
+
abnormalities originating in the perinatal period (P29.1-)
  
, if applicable, congenital Zika virus disease
+
''Excludes2''
  
''Excludes1''
+
specified arrhythmias (I47-I49)
  
Meckel-Gruber syndrome (Q61.9)
+
*'''[[R00.0]]''' Tachycardia, unspecified
  
*'''[[Q03]]''' Congenital hydrocephalus
+
'''Rapid heart beat'''
  
''Includes''
+
Sinoauricular tachycardia NOS
  
hydrocephalus in newborn
+
Sinus (sinusal) tachycardia NOS
  
 
''Excludes1''  
 
''Excludes1''  
  
Arnold-Chiari syndrome, type II (Q07.0-)  
+
neonatal tachycardia (P29.11)
 +
 
 +
paroxysmal tachycardia (I47.-)
 +
 
 +
*'''[[R00.1]]''' Bradycardia, unspecified
  
acquired hydrocephalus (G91.-)
+
Sinoatrial bradycardia
  
hydrocephalus due to congenital toxoplasmosis (P37.1)
+
Sinus bradycardia
  
hydrocephalus with spina bifida (Q05.0-Q05.4)
+
Slow heart beat
  
*'''[[Q03.0]]''' Malformations of aqueduct of Sylvius
+
Vagal bradycardia ''Use additional''  
  
Anomaly of aqueduct of Sylvius
+
code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
  
Obstruction of aqueduct of Sylvius, congenital
+
''Excludes1''
  
Stenosis of aqueduct of Sylvius
+
neonatal bradycardia (P29.12)
  
*'''[[Q03.1]]''' Atresia of foramina of Magendie and Luschka
+
*'''[[R00.2]]''' Palpitations
  
Dandy-Walker syndrome
+
Awareness of heart beat
  
*'''[[Q03.8]]''' Other congenital hydrocephalus
+
*'''[[R00.8]]''' Other abnormalities of heart beat
  
*'''[[Q03.9]]''' Congenital hydrocephalus, unspecified
+
*'''[[R00.9]]''' Unspecified abnormalities of heart beat
  
*'''[[Q04]]''' Other congenital malformations of brain
+
*'''[[R01]]''' Cardiac murmurs and other cardiac sounds
  
 
''Excludes1''  
 
''Excludes1''  
  
cyclopia (Q87.0)  
+
cardiac murmurs and sounds originating in the perinatal period (P29.8)
  
macrocephaly (Q75.3)
+
*'''[[R01.0]]''' Benign and innocent cardiac murmurs
  
*'''[[Q04.0]]''' Congenital malformations of corpus callosum
+
Functional cardiac murmur
  
Agenesis of corpus callosum
+
*'''[[R01.1]]''' Cardiac murmur, unspecified
  
*'''[[Q04.1]]''' Arhinencephaly
+
Cardiac bruit NOS
  
*'''[[Q04.2]]''' Holoprosencephaly
+
Heart murmur NOS
  
*'''[[Q04.3]]''' Other reduction deformities of brain
+
Systolic murmur NOS
  
Absence of part of brain
+
*'''[[R01.2]]''' Other cardiac sounds
  
Agenesis of part of brain
+
Cardiac dullness, increased or decreased
  
Agyria
+
Precordial friction
  
Aplasia of part of brain
+
*'''[[R03]]''' Abnormal blood-pressure reading, without diagnosis
  
Hydranencephaly
+
*'''[[R03.0]]''' Elevated blood-pressure reading, without diagnosis of hypertension
  
Hypoplasia of part of brain
+
Note
  
Lissencephaly
+
This category is to be used to record an episode of elevated blood pressure in a patient in whom no
  
Microgyria
+
formal diagnosis of hypertension has been made, or as an isolated incidental finding
  
Pachygyria
+
*'''[[R03.1]]''' Nonspecific low blood-pressure reading
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital malformations of corpus callosum (Q04.0)
+
hypotension (I95.-)
 +
 
 +
maternal hypotension syndrome (O26.5-)  
  
*'''[[Q04.4]]''' Septo-optic dysplasia of brain
+
neurogenic orthostatic hypotension (G90.3)
  
*'''[[Q04.5]]''' Megalencephaly
+
*'''[[R04]]''' Hemorrhage from respiratory passages
  
*'''[[Q04.6]]''' Congenital cerebral cysts
+
*'''[[R04.0]]''' Epistaxis
  
Porencephaly
+
Hemorrhage from nose
  
Schizencephaly
+
Nosebleed
  
''Excludes1''  
+
*'''[[R04.1]]''' Hemorrhage from throat
  
acquired porencephalic cyst (G93.0)
+
''Excludes2''
  
*'''[[Q04.8]]''' Other specified congenital malformations of brain
+
hemoptysis (R04.2)
  
Arnold-Chiari syndrome, type IV
+
*'''[[R04.2]]''' Hemoptysis
  
Macrogyria
+
Blood-stained sputum
  
*'''[[Q04.9]]''' Congenital malformation of brain, unspecified
+
Cough with hemorrhage
  
Congenital anomaly NOS of brain
+
*'''[[R04.8]]''' Hemorrhage from other sites in respiratory passages
  
Congenital deformity NOS of brain
+
*'''[[R04.81]]''' Acute idiopathic pulmonary hemorrhage in infants
  
Congenital disease or lesion NOS of brain
+
AIPHI
  
Multiple anomalies NOS of brain, congenital
+
Acute idiopathic hemorrhage in infants over 28 days old
  
*'''[[Q05]]''' Spina bifida
+
''Excludes1''  
  
''Includes''
+
perinatal pulmonary hemorrhage (P26.-)
  
hydromeningocele (spinal)  
+
von Willebrand's disease (D68.0)
  
meningocele (spinal)
+
*'''[[R04.89]]''' Hemorrhage from other sites in respiratory passages
  
meningomyelocele
+
Pulmonary hemorrhage NOS
  
myelocele
+
*'''[[R04.9]]''' Hemorrhage from respiratory passages, unspecified
  
myelomeningocele
+
*'''[[R05]]''' Cough
  
rachischisis
+
''Excludes1''
  
spina bifida (aperta)(cystica)  
+
cough with hemorrhage (R04.2)  
  
syringomyelocele ''Use additional'' code for any associated
+
smoker's cough (J41.0)
  
paraplegia (paraparesis) (G82.2-)
+
*'''[[R06]]''' Abnormalities of breathing
  
 
''Excludes1''  
 
''Excludes1''  
  
Arnold-Chiari syndrome, type II (Q07.0-)  
+
acute respiratory distress syndrome (J80)  
  
spina bifida occulta (Q76.0)
+
respiratory arrest (R09.2)  
  
*'''[[Q05.0]]''' Cervical spina bifida with hydrocephalus
+
respiratory arrest of newborn (P28.81)
  
*'''[[Q05.1]]''' Thoracic spina bifida with hydrocephalus
+
respiratory distress syndrome of newborn (P22.-)
  
Dorsal spina bifida with hydrocephalus
+
respiratory failure (J96.-)
  
Thoracolumbar spina bifida with hydrocephalus
+
respiratory failure of newborn (P28.5)
  
*'''[[Q05.2]]''' Lumbar spina bifida with hydrocephalus
+
*'''[[R06.0]]''' Dyspnea
  
Lumbosacral spina bifida with hydrocephalus
+
''Excludes1''
  
*'''[[Q05.3]]''' Sacral spina bifida with hydrocephalus
+
tachypnea NOS (R06.82)
  
*'''[[Q05.4]]''' Unspecified spina bifida with hydrocephalus
+
transient tachypnea of newborn (P22.1)
  
*'''[[Q05.5]]''' Cervical spina bifida without hydrocephalus
+
*'''[[R06.00]]''' Dyspnea, unspecified
  
*'''[[Q05.6]]''' Thoracic spina bifida without hydrocephalus
+
*'''[[R06.01]]''' Orthopnea
  
Dorsal spina bifida NOS
+
*'''[[R06.02]]''' Shortness of breath
  
Thoracolumbar spina bifida NOS
+
*'''[[R06.03]]''' Acute respiratory distress
  
*'''[[Q05.7]]''' Lumbar spina bifida without hydrocephalus
+
*'''[[R06.09]]''' Other forms of dyspnea
  
Lumbosacral spina bifida NOS
+
*'''[[R06.1]]''' Stridor
  
*'''[[Q05.8]]''' Sacral spina bifida without hydrocephalus
+
''Excludes1''  
  
*'''[[Q05.9]]''' Spina bifida, unspecified
+
congenital laryngeal stridor (P28.89)
  
*'''[[Q06]]''' Other congenital malformations of spinal cord
+
laryngismus (stridulus) (J38.5)
  
*'''[[Q06.0]]''' Amyelia
+
*'''[[R06.2]]''' Wheezing
  
*'''[[Q06.1]]''' Hypoplasia and dysplasia of spinal cord
+
''Excludes1''  
  
Atelomyelia
+
Asthma (J45.-)
  
Myelatelia
+
*'''[[R06.3]]''' Periodic breathing
  
Myelodysplasia of spinal cord
+
Cheyne-Stokes breathing
  
*'''[[Q06.2]]''' Diastematomyelia
+
*'''[[R06.4]]''' Hyperventilation
  
*'''[[Q06.3]]''' Other congenital cauda equina malformations
+
''Excludes1''  
  
*'''[[Q06.4]]''' Hydromyelia
+
psychogenic hyperventilation (F45.8)
  
Hydrorachis
+
*'''[[R06.5]]''' Mouth breathing
  
*'''[[Q06.8]]''' Other specified congenital malformations of spinal cord
+
''Excludes2''  
  
*'''[[Q06.9]]''' Congenital malformation of spinal cord, unspecified
+
dry mouth NOS (R68.2)
  
Congenital anomaly NOS of spinal cord
+
*'''[[R06.6]]''' Hiccough
  
Congenital deformity NOS of spinal cord
+
''Excludes1''
  
Congenital disease or lesion NOS of spinal cord
+
psychogenic hiccough (F45.8)
  
*'''[[Q07]]''' Other congenital malformations of nervous system
+
*'''[[R06.7]]''' Sneezing
  
''Excludes2''  
+
*'''[[R06.8]]''' Other abnormalities of breathing
  
congenital central alveolar hypoventilation syndrome (G47.35)
+
*'''[[R06.81]]''' Apnea, not elsewhere classified
  
familial dysautonomia (Riley-Day) (G90.1)
+
Apnea NOS
  
neurofibromatosis (nonmalignant) (Q85.0-)
+
''Excludes1''
  
*'''[[Q07.0]]''' Arnold-Chiari syndrome
+
apnea (of) newborn (P28.4)
  
Arnold-Chiari syndrome, type II
+
sleep apnea (G47.3-)
  
''Excludes1''
+
sleep apnea of newborn (primary) (P28.3)
  
Arnold-Chiari syndrome, type III (Q01.-)
+
*'''[[R06.82]]''' Tachypnea, not elsewhere classified
  
Arnold-Chiari syndrome, type IV (Q04.8)
+
Tachypnea NOS
  
*'''[[Q07.00]]''' Arnold-Chiari syndrome without spina bifida or hydrocephalus
+
''Excludes1''  
  
*'''[[Q07.01]]''' Arnold-Chiari syndrome with spina bifida
+
transitory tachypnea of newborn (P22.1)
  
*'''[[Q07.02]]''' Arnold-Chiari syndrome with hydrocephalus
+
*'''[[R06.83]]''' Snoring
  
*'''[[Q07.03]]''' Arnold-Chiari syndrome with spina bifida and hydrocephalus
+
*'''[[R06.89]]''' Other abnormalities of breathing
  
*'''[[Q07.8]]''' Other specified congenital malformations of nervous system
+
Breath-holding (spells)
  
Agenesis of nerve
+
Sighing
  
Displacement of brachial plexus
+
*'''[[R06.9]]''' Unspecified abnormalities of breathing
  
Jaw-winking syndrome
+
*'''[[R07]]''' Pain in throat and chest
  
Marcus Gunn's syndrome
+
''Excludes1''
  
*'''[[Q07.9]]''' Congenital malformation of nervous system, unspecified
+
epidemic myalgia (B33.0)
  
Congenital anomaly NOS of nervous system
+
''Excludes2''
  
Congenital deformity NOS of nervous system
+
jaw pain R68.84
  
Congenital disease or lesion NOS of nervous system
+
pain in breast (N64.4)
  
Congenital malformations of eye, ear, face and neck (Q10-Q18)
+
*'''[[R07.0]]''' Pain in throat
  
''Excludes2''  
+
''Excludes1''  
  
cleft lip and cleft palate (Q35-Q37)  
+
chronic sore throat (J31.2)  
  
congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)  
+
sore throat (acute) NOS (J02.9)  
  
congenital malformation of larynx (Q31.-)
+
''Excludes2''
  
congenital malformation of lip NEC (Q38.0)  
+
dysphagia (R13.1-)  
  
congenital malformation of nose (Q30.-)  
+
pain in neck (M54.2)
  
congenital malformation of parathyroid gland (Q89.2)
+
*'''[[R07.1]]''' Chest pain on breathing
  
congenital malformation of thyroid gland (Q89.2)
+
Painful respiration
  
*'''[[Q10]]''' Congenital malformations of eyelid, lacrimal apparatus and orbit
+
*'''[[R07.2]]''' Precordial pain
  
''Excludes1''  
+
*'''[[R07.8]]''' Other chest pain
  
cryptophthalmos NOS (Q11.2)
+
*'''[[R07.81]]''' Pleurodynia
  
cryptophthalmos syndrome (Q87.0)
+
Pleurodynia NOS
  
*'''[[Q10.0]]''' Congenital ptosis
+
''Excludes1''  
  
*'''[[Q10.1]]''' Congenital ectropion
+
epidemic pleurodynia (B33.0)
  
*'''[[Q10.2]]''' Congenital entropion
+
*'''[[R07.82]]''' Intercostal pain
  
*'''[[Q10.3]]''' Other congenital malformations of eyelid
+
*'''[[R07.89]]''' Other chest pain
  
Ablepharon
+
Anterior chest-wall pain NOS
  
Blepharophimosis, congenital
+
*'''[[R07.9]]''' Chest pain, unspecified
  
Coloboma of eyelid
+
*'''[[R09]]''' Other symptoms and signs involving the circulatory and respiratory system
  
Congenital absence or agenesis of cilia
+
''Excludes1''
  
Congenital absence or agenesis of eyelid
+
acute respiratory distress syndrome (J80)
  
Congenital accessory eyelid
+
respiratory arrest of newborn (P28.81)
  
Congenital accessory eye muscle
+
respiratory distress syndrome of newborn (P22.0)
  
Congenital malformation of eyelid NOS
+
respiratory failure (J96.-)
  
*'''[[Q10.4]]''' Absence and agenesis of lacrimal apparatus
+
respiratory failure of newborn (P28.5)
  
Congenital absence of punctum lacrimale
+
*'''[[R09.0]]''' Asphyxia and hypoxemia
  
*'''[[Q10.5]]''' Congenital stenosis and stricture of lacrimal duct
+
''Excludes1''  
  
*'''[[Q10.6]]''' Other congenital malformations of lacrimal apparatus
+
asphyxia due to carbon monoxide (T58.-)
  
Congenital malformation of lacrimal apparatus NOS
+
asphyxia due to foreign body in respiratory tract (T17.-)
  
*'''[[Q10.7]]''' Congenital malformation of orbit
+
birth (intrauterine) asphyxia (P84)
  
*'''[[Q11]]''' Anophthalmos, microphthalmos and macrophthalmos
+
hyperventilation (R06.4)
  
*'''[[Q11.0]]''' Cystic eyeball
+
traumatic asphyxia (T71.-)
  
*'''[[Q11.1]]''' Other anophthalmos
+
''Excludes2''  
  
Anophthalmos NOS
+
hypercapnia (R06.89)
  
Agenesis of eye
+
*'''[[R09.01]]''' Asphyxia
  
Aplasia of eye
+
*'''[[R09.02]]''' Hypoxemia
  
*'''[[Q11.2]]''' Microphthalmos
+
*'''[[R09.1]]''' Pleurisy
  
Cryptophthalmos NOS
+
''Excludes1''
  
Dysplasia of eye
+
pleurisy with effusion (J90)
  
Hypoplasia of eye
+
*'''[[R09.2]]''' Respiratory arrest
  
Rudimentary eye
+
Cardiorespiratory failure
  
 
''Excludes1''  
 
''Excludes1''  
  
cryptophthalmos syndrome (Q87.0)
+
cardiac arrest (I46.-)  
 
 
*'''[[Q11.3]]''' Macrophthalmos
 
  
''Excludes1''
+
respiratory arrest of newborn (P28.81)
  
macrophthalmos in congenital glaucoma (Q15.0)
+
respiratory distress of newborn (P22.0)  
  
*'''[[Q12]]''' Congenital lens malformations
+
respiratory failure (J96.-)
  
*'''[[Q12.0]]''' Congenital cataract
+
respiratory failure of newborn (P28.5)
  
*'''[[Q12.1]]''' Congenital displaced lens
+
respiratory insufficiency (R06.89)
  
*'''[[Q12.2]]''' Coloboma of lens
+
respiratory insufficiency of newborn (P28.5)
  
*'''[[Q12.3]]''' Congenital aphakia
+
*'''[[R09.3]]''' Abnormal sputum
  
*'''[[Q12.4]]''' Spherophakia
+
Abnormal amount of sputum
  
*'''[[Q12.8]]''' Other congenital lens malformations
+
Abnormal color of sputum
  
Microphakia
+
Abnormal odor of sputum
  
*'''[[Q12.9]]''' Congenital lens malformation, unspecified
+
Excessive sputum
  
*'''[[Q13]]''' Congenital malformations of anterior segment of eye
+
''Excludes1''  
  
*'''[[Q13.0]]''' Coloboma of iris
+
blood-stained sputum (R04.2)
  
Coloboma NOS
+
*'''[[R09.8]]''' Other specified symptoms and signs involving the circulatory and respiratory systems
  
*'''[[Q13.1]]''' Absence of iris
+
*'''[[R09.81]]''' Nasal congestion
  
Aniridia ''Use additional''  
+
*'''[[R09.82]]''' Postnasal drip
  
code for associated glaucoma (H42)
+
*'''[[R09.89]]''' Other specified symptoms and signs involving the circulatory and respiratory systems
  
*'''[[Q13.2]]''' Other congenital malformations of iris
+
Bruit (arterial)
  
Anisocoria, congenital
+
Abnormal chest percussion
  
Atresia of pupil
+
Feeling of foreign body in throat
  
Congenital malformation of iris NOS
+
Friction sounds in chest
  
Corectopia
+
Chest tympany
  
*'''[[Q13.3]]''' Congenital corneal opacity
+
Choking sensation
  
*'''[[Q13.4]]''' Other congenital corneal malformations
+
'''Rales'''
  
Congenital malformation of cornea NOS
+
Weak pulse
  
Microcornea
+
''Excludes2''
  
Peter's anomaly
+
foreign body in throat (T17.2-)
  
*'''[[Q13.5]]''' Blue sclera
+
wheezing (R06.2)
  
*'''[[Q13.8]]''' Other congenital malformations of anterior segment of eye
+
Symptoms and signs involving the digestive system and abdomen (R10-R19)
  
*'''[[Q13.81]]''' Rieger's anomaly ''Use additional''
+
''Excludes2''  
  
code for associated glaucoma (H42)
+
congenital or infantile pylorospasm (Q40.0)  
  
*'''[[Q13.89]]''' Other congenital malformations of anterior segment of eye
+
gastrointestinal hemorrhage (K92.0-K92.2)
  
*'''[[Q13.9]]''' Congenital malformation of anterior segment of eye, unspecified
+
intestinal obstruction (K56.-)
  
*'''[[Q14]]''' Congenital malformations of posterior segment of eye
+
newborn gastrointestinal hemorrhage (P54.0-P54.3)
  
''Excludes2''
+
newborn intestinal obstruction (P76.-)
  
optic nerve hypoplasia (H47.03-)
+
pylorospasm (K31.3)  
  
*'''[[Q14.0]]''' Congenital malformation of vitreous humor
+
signs and symptoms involving the urinary system (R30-R39)
  
Congenital vitreous opacity
+
symptoms referable to female genital organs (N94.-)
  
*'''[[Q14.1]]''' Congenital malformation of retina
+
symptoms referable to male genital organs (N48-N50)
  
Congenital retinal aneurysm
+
*'''[[R10]]''' Abdominal and pelvic pain
  
*'''[[Q14.2]]''' Congenital malformation of optic disc
+
''Excludes1''  
  
Coloboma of optic disc
+
renal colic (N23)
  
*'''[[Q14.3]]''' Congenital malformation of choroid
+
''Excludes2''  
  
*'''[[Q14.8]]''' Other congenital malformations of posterior segment of eye
+
dorsalgia (M54.-)
  
Coloboma of the fundus
+
flatulence and related conditions (R14.-)
  
*'''[[Q14.9]]''' Congenital malformation of posterior segment of eye, unspecified
+
*'''[[R10.0]]''' Acute abdomen
  
*'''[[Q15]]''' Other congenital malformations of eye
+
Severe abdominal pain (generalized) (with abdominal rigidity)
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital nystagmus (H55.01)  
+
abdominal rigidity NOS (R19.3)  
  
ocular albinism (E70.31-)  
+
generalized abdominal pain NOS (R10.84)  
  
optic nerve hypoplasia (H47.03-)  
+
localized abdominal pain (R10.1-R10.3-)
  
retinitis pigmentosa (H35.52)
+
*'''[[R10.1]]''' Pain localized to upper abdomen
  
*'''[[Q15.0]]''' Congenital glaucoma
+
*'''[[R10.10]]''' Upper abdominal pain, unspecified
  
Axenfeld's anomaly
+
*'''[[R10.11]]''' Right upper quadrant pain
  
Buphthalmos
+
*'''[[R10.12]]''' Left upper quadrant pain
  
Glaucoma of childhood
+
*'''[[R10.13]]''' Epigastric pain
  
Glaucoma of newborn
+
Dyspepsia
  
Hydrophthalmos
+
''Excludes1''
  
Keratoglobus, congenital, with glaucoma
+
functional dyspepsia (K30)
  
Macrocornea with glaucoma
+
*'''[[R10.2]]''' Pelvic and perineal pain
  
Macrophthalmos in congenital glaucoma
+
''Excludes1''
  
Megalocornea with glaucoma
+
vulvodynia (N94.81)
  
*'''[[Q15.8]]''' Other specified congenital malformations of eye
+
*'''[[R10.3]]''' Pain localized to other parts of lower abdomen
  
*'''[[Q15.9]]''' Congenital malformation of eye, unspecified
+
*'''[[R10.30]]''' Lower abdominal pain, unspecified
  
Congenital anomaly of eye
+
*'''[[R10.31]]''' Right lower quadrant pain
  
Congenital deformity of eye
+
*'''[[R10.32]]''' Left lower quadrant pain
  
*'''[[Q16]]''' Congenital malformations of ear causing impairment of hearing
+
*'''[[R10.33]]''' Periumbilical pain
  
''Excludes1''  
+
*'''[[R10.8]]''' Other abdominal pain
  
congenital deafness (H90.-)
+
*'''[[R10.81]]''' Abdominal tenderness
  
*'''[[Q16.0]]''' Congenital absence of (ear) auricle
+
Abdominal tenderness NOS
  
*'''[[Q16.1]]''' Congenital absence, atresia and stricture of auditory canal (external)
+
*'''[[R10.811]]''' Right upper quadrant abdominal tenderness
  
Congenital atresia or stricture of osseous meatus
+
*'''[[R10.812]]''' Left upper quadrant abdominal tenderness
  
*'''[[Q16.2]]''' Absence of eustachian tube
+
*'''[[R10.813]]''' Right lower quadrant abdominal tenderness
  
*'''[[Q16.3]]''' Congenital malformation of ear ossicles
+
*'''[[R10.814]]''' Left lower quadrant abdominal tenderness
  
Congenital fusion of ear ossicles
+
*'''[[R10.815]]''' Periumbilic abdominal tenderness
  
*'''[[Q16.4]]''' Other congenital malformations of middle ear
+
*'''[[R10.816]]''' Epigastric abdominal tenderness
  
Congenital malformation of middle ear NOS
+
*'''[[R10.817]]''' Generalized abdominal tenderness
  
*'''[[Q16.5]]''' Congenital malformation of inner ear
+
*'''[[R10.819]]''' Abdominal tenderness, unspecified site
  
Congenital anomaly of membranous labyrinth
+
*'''[[R10.82]]''' Rebound abdominal tenderness
  
Congenital anomaly of organ of Corti
+
*'''[[R10.821]]''' Right upper quadrant rebound abdominal tenderness
  
*'''[[Q16.9]]''' Congenital malformation of ear causing impairment of hearing, unspecified
+
*'''[[R10.822]]''' Left upper quadrant rebound abdominal tenderness
  
Congenital absence of ear NOS
+
*'''[[R10.823]]''' Right lower quadrant rebound abdominal tenderness
  
*'''[[Q17]]''' Other congenital malformations of ear
+
*'''[[R10.824]]''' Left lower quadrant rebound abdominal tenderness
  
''Excludes1''  
+
*'''[[R10.825]]''' Periumbilic rebound abdominal tenderness
  
congenital malformations of ear with impairment of hearing (Q16.0-Q16.9)
+
*'''[[R10.826]]''' Epigastric rebound abdominal tenderness
  
preauricular sinus (Q18.1)
+
*'''[[R10.827]]''' Generalized rebound abdominal tenderness
  
*'''[[Q17.0]]''' Accessory auricle
+
*'''[[R10.829]]''' Rebound abdominal tenderness, unspecified site
  
Accessory tragus
+
*'''[[R10.83]]''' Colic
  
Polyotia
+
Colic NOS
  
Preauricular appendage or tag
+
Infantile colic
  
Supernumerary ear
+
''Excludes1''
  
Supernumerary lobule
+
colic in adult and child over 12 months old (R10.84)
  
*'''[[Q17.1]]''' Macrotia
+
*'''[[R10.84]]''' Generalized abdominal pain
  
*'''[[Q17.2]]''' Microtia
+
''Excludes1''  
 
 
*'''[[Q17.3]]''' Other misshapen ear
 
  
Pointed ear
+
generalized abdominal pain associated with acute abdomen (R10.0)
  
*'''[[Q17.4]]''' Misplaced ear
+
*'''[[R10.9]]''' Unspecified abdominal pain
  
Low-set ears
+
*'''[[R11]]''' Nausea and vomiting
  
 
''Excludes1''  
 
''Excludes1''  
  
cervical auricle (Q18.2)
+
cyclical vomiting associated with migraine (G43.A-)  
  
*'''[[Q17.5]]''' Prominent ear
+
excessive vomiting in pregnancy (O21.-)
  
Bat ear
+
hematemesis (K92.0)
  
*'''[[Q17.8]]''' Other specified congenital malformations of ear
+
neonatal hematemesis (P54.0)
  
Congenital absence of lobe of ear
+
newborn vomiting (P92.0-)
  
*'''[[Q17.9]]''' Congenital malformation of ear, unspecified
+
psychogenic vomiting (F50.89)
  
Congenital anomaly of ear NOS
+
vomiting associated with bulimia nervosa (F50.2)
  
*'''[[Q18]]''' Other congenital malformations of face and neck
+
vomiting following gastrointestinal surgery (K91.0)
  
''Excludes1''  
+
*'''[[R11.0]]''' Nausea
  
cleft lip and cleft palate (Q35-Q37)
+
Nausea NOS
  
conditions classified to Q67.0-Q67.4
+
Nausea without vomiting
  
congenital malformations of skull and face bones (Q75.-)
+
*'''[[R11.1]]''' Vomiting
  
cyclopia (Q87.0)
+
*'''[[R11.10]]''' Vomiting, unspecified
  
dentofacial anomalies (including malocclusion) (M26.-)
+
Vomiting NOS
  
malformation syndromes affecting facial appearance (Q87.0)
+
*'''[[R11.11]]''' Vomiting without nausea
  
persistent thyroglossal duct (Q89.2)
+
*'''[[R11.12]]''' Projectile vomiting
  
*'''[[Q18.0]]''' Sinus, fistula and cyst of branchial cleft
+
*'''[[R11.13]]''' Vomiting of fecal matter
  
Branchial vestige
+
*'''[[R11.14]]''' Bilious vomiting
  
*'''[[Q18.1]]''' Preauricular sinus and cyst
+
Bilious emesis
  
Fistula of auricle, congenital
+
*'''[[R11.15]]''' Cyclical vomiting syndrome unrelated to migraine
  
Cervicoaural fistula
+
Cyclic vomiting syndrome NOS
  
*'''[[Q18.2]]''' Other branchial cleft malformations
+
Persistent vomiting
  
Branchial cleft malformation NOS
+
''Excludes1''
  
Cervical auricle
+
cyclical vomiting in migraine (G43.A-)
  
Otocephaly
+
''Excludes2''
  
*'''[[Q18.3]]''' Webbing of neck
+
bulimia nervosa (F50.2)
  
Pterygium colli
+
diabetes mellitus due to underlying condition (E08.-)
  
*'''[[Q18.4]]''' Macrostomia
+
*'''[[R11.2]]''' Nausea with vomiting, unspecified
  
*'''[[Q18.5]]''' Microstomia
+
Persistent nausea with vomiting NOS
  
*'''[[Q18.6]]''' Macrocheilia
+
*'''[[R12]]''' Heartburn
  
Hypertrophy of lip, congenital
+
''Excludes1''
  
*'''[[Q18.7]]''' Microcheilia
+
dyspepsia NOS (R10.13)
  
*'''[[Q18.8]]''' Other specified congenital malformations of face and neck
+
functional dyspepsia (K30)
  
Medial cyst of face and neck
+
*'''[[R13]]''' Aphagia and dysphagia
  
Medial fistula of face and neck
+
*'''[[R13.0]]''' Aphagia
  
Medial sinus of face and neck
+
Inability to swallow
  
*'''[[Q18.9]]''' Congenital malformation of face and neck, unspecified
+
''Excludes1''  
  
Congenital anomaly NOS of face and neck
+
psychogenic aphagia (F50.9)
  
Congenital malformations of the circulatory system (Q20-Q28)
+
*'''[[R13.1]]''' Dysphagia ''Code first''
  
*'''[[Q20]]''' Congenital malformations of cardiac chambers and connections
+
, if applicable, dysphagia following cerebrovascular disease (I69. with final characters -91)
  
 
''Excludes1''  
 
''Excludes1''  
  
dextrocardia with situs inversus (Q89.3)  
+
psychogenic dysphagia (F45.8)
  
mirror-image atrial arrangement with situs inversus (Q89.3)
+
*'''[[R13.10]]''' Dysphagia, unspecified
  
*'''[[Q20.0]]''' Common arterial trunk
+
Difficulty in swallowing NOS
  
Persistent truncus arteriosus
+
*'''[[R13.11]]''' Dysphagia, oral phase
  
''Excludes1''  
+
*'''[[R13.12]]''' Dysphagia, oropharyngeal phase
  
aortic septal defect (Q21.4)
+
*'''[[R13.13]]''' Dysphagia, pharyngeal phase
  
*'''[[Q20.1]]''' Double outlet right ventricle
+
*'''[[R13.14]]''' Dysphagia, pharyngoesophageal phase
  
Taussig-Bing syndrome
+
*'''[[R13.19]]''' Other dysphagia
  
*'''[[Q20.2]]''' Double outlet left ventricle
+
Cervical dysphagia
  
*'''[[Q20.3]]''' Discordant ventriculoarterial connection
+
Neurogenic dysphagia
  
Dextrotransposition of aorta
+
*'''[[R14]]''' Flatulence and related conditions
  
Transposition of great vessels (complete)
+
''Excludes1''
  
*'''[[Q20.4]]''' Double inlet ventricle
+
psychogenic aerophagy (F45.8)
  
Common ventricle
+
*'''[[R14.0]]''' Abdominal distension (gaseous)
  
Cor triloculare biatriatum
+
Bloating
  
Single ventricle
+
Tympanites (abdominal) (intestinal)
  
*'''[[Q20.5]]''' Discordant atrioventricular connection
+
*'''[[R14.1]]''' Gas pain
  
Corrected transposition
+
*'''[[R14.2]]''' Eructation
  
Levotransposition
+
*'''[[R14.3]]''' Flatulence
  
Ventricular inversion
+
*'''[[R15]]''' Fecal incontinence
  
*'''[[Q20.6]]''' Isomerism of atrial appendages
+
''Includes''  
  
Isomerism of atrial appendages with asplenia or polysplenia
+
encopresis NOS
  
*'''[[Q20.8]]''' Other congenital malformations of cardiac chambers and connections
+
''Excludes1''  
 
 
Cor binoculare
 
  
*'''[[Q20.9]]''' Congenital malformation of cardiac chambers and connections, unspecified
+
fecal incontinence of nonorganic origin (F98.1)
  
*'''[[Q21]]''' Congenital malformations of cardiac septa
+
*'''[[R15.0]]''' Incomplete defecation
  
 
''Excludes1''  
 
''Excludes1''  
  
acquired cardiac septal defect (I51.0)
+
constipation (K59.0-)  
  
*'''[[Q21.0]]''' Ventricular septal defect
+
fecal impaction (K56.41)
  
Roger's disease
+
*'''[[R15.1]]''' Fecal smearing
  
*'''[[Q21.1]]''' Atrial septal defect
+
Fecal soiling
  
Coronary sinus defect
+
*'''[[R15.2]]''' Fecal urgency
  
Patent or persistent foramen ovale
+
*'''[[R15.9]]''' Full incontinence of feces
  
Patent or persistent ostium secundum defect (type II)
+
Fecal incontinence NOS
  
Patent or persistent sinus venosus defect
+
*'''[[R16]]''' Hepatomegaly and splenomegaly, not elsewhere classified
  
*'''[[Q21.2]]''' Atrioventricular septal defect
+
*'''[[R16.0]]''' Hepatomegaly, not elsewhere classified
  
Common atrioventricular canal
+
Hepatomegaly NOS
  
Endocardial cushion defect
+
*'''[[R16.1]]''' Splenomegaly, not elsewhere classified
  
Ostium primum atrial septal defect (type I)
+
Splenomegaly NOS
  
*'''[[Q21.3]]''' Tetralogy of Fallot
+
*'''[[R16.2]]''' Hepatomegaly with splenomegaly, not elsewhere classified
  
Ventricular septal defect with pulmonary stenosis or atresia, dextroposition of aorta and hypertrophy of right
+
Hepatosplenomegaly NOS
  
ventricle
+
*'''[[R17]]''' Unspecified jaundice
  
*'''[[Q21.4]]''' Aortopulmonary septal defect
+
''Excludes1''  
  
Aortic septal defect
+
neonatal jaundice (P55, P57-P59)
  
Aortopulmonary window
+
*'''[[R18]]''' Ascites
  
*'''[[Q21.8]]''' Other congenital malformations of cardiac septa
+
''Includes''  
  
Eisenmenger's defect
+
fluid in peritoneal cavity
  
Pentalogy of Fallot ''Code also''  
+
''Excludes1''  
  
if applicable
+
ascites in alcoholic cirrhosis (K70.31)
  
Eisenmenger's complex (I27.83)  
+
ascites in alcoholic hepatitis (K70.11)  
  
Eisenmenger's syndrome (I27.83)
+
ascites in toxic liver disease with chronic active hepatitis (K71.51)
  
*'''[[Q21.9]]''' Congenital malformation of cardiac septum, unspecified
+
*'''[[R18.0]]''' Malignant ascites ''Code first''
  
Septal (heart) defect NOS
+
malignancy, such as
  
*'''[[Q22]]''' Congenital malformations of pulmonary and tricuspid valves
+
malignant neoplasm of ovary (C56.-)
  
*'''[[Q22.0]]''' Pulmonary valve atresia
+
secondary malignant neoplasm of retroperitoneum and peritoneum (C78.6)
  
*'''[[Q22.1]]''' Congenital pulmonary valve stenosis
+
*'''[[R18.8]]''' Other ascites
  
*'''[[Q22.2]]''' Congenital pulmonary valve insufficiency
+
Ascites NOS
  
Congenital pulmonary valve regurgitation
+
Peritoneal effusion (chronic)
  
*'''[[Q22.3]]''' Other congenital malformations of pulmonary valve
+
*'''[[R19]]''' Other symptoms and signs involving the digestive system and abdomen
  
Congenital malformation of pulmonary valve NOS
+
''Excludes1''
  
Supernumerary cusps of pulmonary valve
+
acute abdomen (R10.0)
  
*'''[[Q22.4]]''' Congenital tricuspid stenosis
+
*'''[[R19.0]]''' Intra-abdominal and pelvic swelling, mass and lump
  
Congenital tricuspid atresia
+
''Excludes1''
  
*'''[[Q22.5]]''' Ebstein's anomaly
+
abdominal distension (gaseous) (R14.-)
  
*'''[[Q22.6]]''' Hypoplastic right heart syndrome
+
ascites (R18.-)
  
*'''[[Q22.8]]''' Other congenital malformations of tricuspid valve
+
*'''[[R19.00]]''' Intra-abdominal and pelvic swelling, mass and lump, unspecified site
  
*'''[[Q22.9]]''' Congenital malformation of tricuspid valve, unspecified
+
*'''[[R19.01]]''' Right upper quadrant abdominal swelling, mass and lump
  
*'''[[Q23]]''' Congenital malformations of aortic and mitral valves
+
*'''[[R19.02]]''' Left upper quadrant abdominal swelling, mass and lump
  
*'''[[Q23.0]]''' Congenital stenosis of aortic valve
+
*'''[[R19.03]]''' Right lower quadrant abdominal swelling, mass and lump
  
Congenital aortic atresia
+
*'''[[R19.04]]''' Left lower quadrant abdominal swelling, mass and lump
  
Congenital aortic stenosis NOS
+
*'''[[R19.05]]''' Periumbilic swelling, mass or lump
  
''Excludes1''
+
Diffuse or generalized umbilical swelling or mass
  
congenital stenosis of aortic valve in hypoplastic left heart syndrome (Q23.4)
+
*'''[[R19.06]]''' Epigastric swelling, mass or lump
  
congenital subaortic stenosis (Q24.4)
+
*'''[[R19.07]]''' Generalized intra-abdominal and pelvic swelling, mass and lump
  
supravalvular aortic stenosis (congenital) (Q25.3)
+
Diffuse or generalized intra-abdominal swelling or mass NOS
  
*'''[[Q23.1]]''' Congenital insufficiency of aortic valve
+
Diffuse or generalized pelvic swelling or mass NOS
  
Bicuspid aortic valve
+
*'''[[R19.09]]''' Other intra-abdominal and pelvic swelling, mass and lump
  
Congenital aortic insufficiency
+
*'''[[R19.1]]''' Abnormal bowel sounds
  
*'''[[Q23.2]]''' Congenital mitral stenosis
+
*'''[[R19.11]]''' Absent bowel sounds
  
Congenital mitral atresia
+
*'''[[R19.12]]''' Hyperactive bowel sounds
  
*'''[[Q23.3]]''' Congenital mitral insufficiency
+
*'''[[R19.15]]''' Other abnormal bowel sounds
  
*'''[[Q23.4]]''' Hypoplastic left heart syndrome
+
Abnormal bowel sounds NOS
  
*'''[[Q23.8]]''' Other congenital malformations of aortic and mitral valves
+
*'''[[R19.2]]''' Visible peristalsis
  
*'''[[Q23.9]]''' Congenital malformation of aortic and mitral valves, unspecified
+
Hyperperistalsis
  
*'''[[Q24]]''' Other congenital malformations of heart
+
*'''[[R19.3]]''' Abdominal rigidity
  
 
''Excludes1''  
 
''Excludes1''  
  
endocardial fibroelastosis (I42.4)
+
abdominal rigidity with severe abdominal pain (R10.0)
  
*'''[[Q24.0]]''' Dextrocardia
+
*'''[[R19.30]]''' Abdominal rigidity, unspecified site
  
''Excludes1''  
+
*'''[[R19.31]]''' Right upper quadrant abdominal rigidity
  
dextrocardia with situs inversus (Q89.3)
+
*'''[[R19.32]]''' Left upper quadrant abdominal rigidity
  
isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
+
*'''[[R19.33]]''' Right lower quadrant abdominal rigidity
  
mirror-image atrial arrangement with situs inversus (Q89.3)
+
*'''[[R19.34]]''' Left lower quadrant abdominal rigidity
  
*'''[[Q24.1]]''' Levocardia
+
*'''[[R19.35]]''' Periumbilic abdominal rigidity
  
*'''[[Q24.2]]''' Cor triatriatum
+
*'''[[R19.36]]''' Epigastric abdominal rigidity
  
*'''[[Q24.3]]''' Pulmonary infundibular stenosis
+
*'''[[R19.37]]''' Generalized abdominal rigidity
  
Subvalvular pulmonic stenosis
+
*'''[[R19.4]]''' Change in bowel habit
  
*'''[[Q24.4]]''' Congenital subaortic stenosis
+
''Excludes1''  
  
*'''[[Q24.5]]''' Malformation of coronary vessels
+
constipation (K59.0-)
  
Congenital coronary (artery) aneurysm
+
functional diarrhea (K59.1)
  
*'''[[Q24.6]]''' Congenital heart block
+
*'''[[R19.5]]''' Other fecal abnormalities
  
*'''[[Q24.8]]''' Other specified congenital malformations of heart
+
Abnormal stool color
  
Congenital diverticulum of left ventricle
+
Bulky stools
  
Congenital malformation of myocardium
+
Mucus in stools
  
Congenital malformation of pericardium
+
Occult blood in feces
  
Malposition of heart
+
Occult blood in stools
  
Uhl's disease
+
''Excludes1''
  
*'''[[Q24.9]]''' Congenital malformation of heart, unspecified
+
melena (K92.1)
  
Congenital anomaly of heart
+
neonatal melena (P54.1)
  
Congenital disease of heart
+
*'''[[R19.6]]''' Halitosis
  
*'''[[Q25]]''' Congenital malformations of great arteries
+
*'''[[R19.7]]''' Diarrhea, unspecified
  
*'''[[Q25.0]]''' Patent ductus arteriosus
+
Diarrhea NOS
  
Patent ductus Botallo
+
''Excludes1''
  
Persistent ductus arteriosus
+
functional diarrhea (K59.1)
  
*'''[[Q25.1]]''' Coarctation of aorta
+
neonatal diarrhea (P78.3)
  
Coarctation of aorta (preductal) (postductal)
+
psychogenic diarrhea (F45.8)
  
Stenosis of aorta
+
*'''[[R19.8]]''' Other specified symptoms and signs involving the digestive system and abdomen
  
*'''[[Q25.2]]''' Atresia of aorta
+
Symptoms and signs involving the skin and subcutaneous tissue (R20-R23)
  
*'''[[Q25.21]]''' Interruption of aortic arch
+
''Excludes2''  
  
Atresia of aortic arch
+
symptoms relating to breast (N64.4-N64.5)
  
*'''[[Q25.29]]''' Other atresia of aorta
+
*'''[[R20]]''' Disturbances of skin sensation
  
Atresia of aorta
+
''Excludes1''
  
*'''[[Q25.3]]''' Supravalvular aortic stenosis
+
dissociative anesthesia and sensory loss (F44.6)
  
''Excludes1''
+
psychogenic disturbances (F45.8)
  
congenital aortic stenosis NOS (Q23.0)
+
*'''[[R20.0]]''' Anesthesia of skin
  
congenital stenosis of aortic valve (Q23.0)
+
*'''[[R20.1]]''' Hypoesthesia of skin
  
*'''[[Q25.4]]''' Other congenital malformations of aorta
+
*'''[[R20.2]]''' Paresthesia of skin
  
''Excludes1''
+
Formication
  
hypoplasia of aorta in hypoplastic left heart syndrome (Q23.4)
+
Pins and needles
  
*'''[[Q25.40]]''' Congenital malformation of aorta unspecified
+
Tingling skin
  
*'''[[Q25.41]]''' Absence and aplasia of aorta
+
''Excludes1''  
  
*'''[[Q25.42]]''' Hypoplasia of aorta
+
acroparesthesia (I73.8)
  
*'''[[Q25.43]]''' Congenital aneurysm of aorta
+
*'''[[R20.3]]''' Hyperesthesia
  
Congenital aneurysm of aortic root
+
*'''[[R20.8]]''' Other disturbances of skin sensation
  
Congenital aneurysm of aortic sinus
+
*'''[[R20.9]]''' Unspecified disturbances of skin sensation
  
*'''[[Q25.44]]''' Congenital dilation of aorta
+
*'''[[R21]]''' Rash and other nonspecific skin eruption
  
*'''[[Q25.45]]''' Double aortic arch
+
''Includes''  
  
Vascular ring of aorta
+
rash NOS
  
*'''[[Q25.46]]''' Tortuous aortic arch
+
''Excludes1''  
  
Persistent convolutions of aortic arch
+
specified type of rash- code to condition
  
*'''[[Q25.47]]''' Right aortic arch
+
vesicular eruption (R23.8)
  
Persistent right aortic arch
+
*'''[[R22]]''' Localized swelling, mass and lump of skin and subcutaneous tissue
  
*'''[[Q25.48]]''' Anomalous origin of subclavian artery
+
''Includes''  
  
*'''[[Q25.49]]''' Other congenital malformations of aorta
+
subcutaneous nodules (localized)(superficial)
  
Aortic arch
+
''Excludes1''
  
Bovine arch
+
abnormal findings on diagnostic imaging (R90-R93)
  
*'''[[Q25.5]]''' Atresia of pulmonary artery
+
edema (R60.-)
  
*'''[[Q25.6]]''' Stenosis of pulmonary artery
+
enlarged lymph nodes (R59.-)
  
Supravalvular pulmonary stenosis
+
localized adiposity (E65)
  
*'''[[Q25.7]]''' Other congenital malformations of pulmonary artery
+
swelling of joint (M25.4-)
  
*'''[[Q25.71]]''' Coarctation of pulmonary artery
+
*'''[[R22.0]]''' Localized swelling, mass and lump, head
  
*'''[[Q25.72]]''' Congenital pulmonary arteriovenous malformation
+
*'''[[R22.1]]''' Localized swelling, mass and lump, neck
  
Congenital pulmonary arteriovenous aneurysm
+
*'''[[R22.2]]''' Localized swelling, mass and lump, trunk
  
*'''[[Q25.79]]''' Other congenital malformations of pulmonary artery
+
''Excludes1''  
  
Aberrant pulmonary artery
+
intra-abdominal or pelvic mass and lump (R19.0-)
  
Agenesis of pulmonary artery
+
intra-abdominal or pelvic swelling (R19.0-)
  
Congenital aneurysm of pulmonary artery
+
''Excludes2''
  
Congenital anomaly of pulmonary artery
+
breast mass and lump (N63)
  
Hypoplasia of pulmonary artery
+
*'''[[R22.3]]''' Localized swelling, mass and lump, upper limb
  
*'''[[Q25.8]]''' Other congenital malformations of other great arteries
+
*'''[[R22.30]]''' Localized swelling, mass and lump, unspecified upper limb
  
*'''[[Q25.9]]''' Congenital malformation of great arteries, unspecified
+
*'''[[R22.31]]''' Localized swelling, mass and lump, right upper limb
  
*'''[[Q26]]''' Congenital malformations of great veins
+
*'''[[R22.32]]''' Localized swelling, mass and lump, left upper limb
  
*'''[[Q26.0]]''' Congenital stenosis of vena cava
+
*'''[[R22.33]]''' Localized swelling, mass and lump, upper limb, bilateral
  
Congenital stenosis of vena cava (inferior)(superior)
+
*'''[[R22.4]]''' Localized swelling, mass and lump, lower limb
  
*'''[[Q26.1]]''' Persistent left superior vena cava
+
*'''[[R22.40]]''' Localized swelling, mass and lump, unspecified lower limb
  
*'''[[Q26.2]]''' Total anomalous pulmonary venous connection
+
*'''[[R22.41]]''' Localized swelling, mass and lump, right lower limb
  
Total anomalous pulmonary venous return (TAPVR), subdiaphragmatic
+
*'''[[R22.42]]''' Localized swelling, mass and lump, left lower limb
  
Total anomalous pulmonary venous return (TAPVR), supradiaphragmatic
+
*'''[[R22.43]]''' Localized swelling, mass and lump, lower limb, bilateral
  
*'''[[Q26.3]]''' Partial anomalous pulmonary venous connection
+
*'''[[R22.9]]''' Localized swelling, mass and lump, unspecified
  
Partial anomalous pulmonary venous return
+
*'''[[R23]]''' Other skin changes
  
*'''[[Q26.4]]''' Anomalous pulmonary venous connection, unspecified
+
*'''[[R23.0]]''' Cyanosis
  
*'''[[Q26.5]]''' Anomalous portal venous connection
+
''Excludes1''  
  
*'''[[Q26.6]]''' Portal vein-hepatic artery fistula
+
acrocyanosis (I73.8)
  
*'''[[Q26.8]]''' Other congenital malformations of great veins
+
cyanotic attacks of newborn (P28.2)
  
Absence of vena cava (inferior) (superior)
+
*'''[[R23.1]]''' Pallor
  
Azygos continuation of inferior vena cava
+
Clammy skin
  
Persistent left posterior cardinal vein
+
*'''[[R23.2]]''' Flushing
  
Scimitar syndrome
+
Excessive blushing ''Code first''
  
*'''[[Q26.9]]''' Congenital malformation of great vein, unspecified
+
, if applicable, menopausal and female climacteric states (N95.1)
  
Congenital anomaly of vena cava (inferior) (superior) NOS
+
*'''[[R23.3]]''' Spontaneous ecchymoses
  
*'''[[Q27]]''' Other congenital malformations of peripheral vascular system
+
Petechiae
  
''Excludes2''  
+
''Excludes1''  
  
anomalies of cerebral and precerebral vessels (Q28.0-Q28.3)  
+
ecchymoses of newborn (P54.5)  
  
anomalies of coronary vessels (Q24.5)  
+
purpura (D69.-)
  
anomalies of pulmonary artery (Q25.5-Q25.7)
+
*'''[[R23.4]]''' Changes in skin texture
  
congenital retinal aneurysm (Q14.1)
+
Desquamation of skin
  
hemangioma and lymphangioma (D18.-)
+
Induration of skin
  
*'''[[Q27.0]]''' Congenital absence and hypoplasia of umbilical artery
+
Scaling of skin
  
Single umbilical artery
+
''Excludes1''  
 
 
*'''[[Q27.1]]''' Congenital renal artery stenosis
 
  
*'''[[Q27.2]]''' Other congenital malformations of renal artery
+
epidermal thickening NOS (L85.9)
  
Congenital malformation of renal artery NOS
+
*'''[[R23.8]]''' Other skin changes
  
Multiple renal arteries
+
*'''[[R23.9]]''' Unspecified skin changes
  
*'''[[Q27.3]]''' Arteriovenous malformation (peripheral)
+
Symptoms and signs involving the nervous and musculoskeletal systems (R25-R29)
  
Arteriovenous aneurysm
+
*'''[[R25]]''' Abnormal involuntary movements
  
 
''Excludes1''  
 
''Excludes1''  
  
acquired arteriovenous aneurysm (I77.0)  
+
specific movement disorders (G20-G26)  
  
''Excludes2''
+
stereotyped movement disorders (F98.4)
  
arteriovenous malformation of cerebral vessels (Q28.2)  
+
tic disorders (F95.-)
  
arteriovenous malformation of precerebral vessels (Q28.0)
+
*'''[[R25.0]]''' Abnormal head movements
  
*'''[[Q27.30]]''' Arteriovenous malformation, site unspecified
+
*'''[[R25.1]]''' Tremor, unspecified
  
*'''[[Q27.31]]''' Arteriovenous malformation of vessel of upper limb
+
''Excludes1''  
  
*'''[[Q27.32]]''' Arteriovenous malformation of vessel of lower limb
+
chorea NOS (G25.5)
  
*'''[[Q27.33]]''' Arteriovenous malformation of digestive system vessel
+
essential tremor (G25.0)
  
*'''[[Q27.34]]''' Arteriovenous malformation of renal vessel
+
hysterical tremor (F44.4)
  
*'''[[Q27.39]]''' Arteriovenous malformation, other site
+
intention tremor (G25.2)
  
*'''[[Q27.4]]''' Congenital phlebectasia
+
*'''[[R25.2]]''' Cramp and spasm
  
*'''[[Q27.8]]''' Other specified congenital malformations of peripheral vascular system
+
''Excludes2''  
  
Absence of peripheral vascular system
+
carpopedal spasm (R29.0)
  
Atresia of peripheral vascular system
+
charley-horse (M62.831)
  
Congenital aneurysm (peripheral)  
+
infantile spasms (G40.4-)  
  
Congenital stricture, artery
+
muscle spasm of back (M62.830)
  
Congenital varix
+
muscle spasm of calf (M62.831)
  
''Excludes1''  
+
*'''[[R25.3]]''' Fasciculation
  
arteriovenous malformation (Q27.3-)
+
Twitching NOS
  
*'''[[Q27.9]]''' Congenital malformation of peripheral vascular system, unspecified
+
*'''[[R25.8]]''' Other abnormal involuntary movements
  
Anomaly of artery or vein NOS
+
*'''[[R25.9]]''' Unspecified abnormal involuntary movements
  
*'''[[Q28]]''' Other congenital malformations of circulatory system
+
*'''[[R26]]''' Abnormalities of gait and mobility
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital aneurysm NOS (Q27.8)  
+
ataxia NOS (R27.0)  
  
congenital coronary aneurysm (Q24.5)  
+
hereditary ataxia (G11.-)  
  
ruptured cerebral arteriovenous malformation (I60.8)  
+
locomotor (syphilitic) ataxia (A52.11)  
  
ruptured malformation of precerebral vessels (I72.0)  
+
immobility syndrome (paraplegic) (M62.3)
  
''Excludes2''  
+
*'''[[R26.0]]''' Ataxic gait
  
congenital peripheral aneurysm (Q27.8)
+
Staggering gait
  
congenital pulmonary aneurysm (Q25.79)
+
*'''[[R26.1]]''' Paralytic gait
  
congenital retinal aneurysm (Q14.1)
+
Spastic gait
  
*'''[[Q28.0]]''' Arteriovenous malformation of precerebral vessels
+
*'''[[R26.2]]''' Difficulty in walking, not elsewhere classified
  
Congenital arteriovenous precerebral aneurysm (nonruptured)
+
''Excludes1''
  
*'''[[Q28.1]]''' Other malformations of precerebral vessels
+
falling (R29.6)
  
Congenital malformation of precerebral vessels NOS
+
unsteadiness on feet (R26.81)
  
Congenital precerebral aneurysm (nonruptured)
+
*'''[[R26.8]]''' Other abnormalities of gait and mobility
  
*'''[[Q28.2]]''' Arteriovenous malformation of cerebral vessels
+
*'''[[R26.81]]''' Unsteadiness on feet
  
Arteriovenous malformation of brain NOS
+
*'''[[R26.89]]''' Other abnormalities of gait and mobility
  
Congenital arteriovenous cerebral aneurysm (nonruptured)
+
*'''[[R26.9]]''' Unspecified abnormalities of gait and mobility
  
*'''[[Q28.3]]''' Other malformations of cerebral vessels
+
*'''[[R27]]''' Other lack of coordination
  
Congenital cerebral aneurysm (nonruptured)
+
''Excludes1''
  
Congenital malformation of cerebral vessels NOS
+
ataxic gait (R26.0)
  
Developmental venous anomaly
+
hereditary ataxia (G11.-)
  
*'''[[Q28.8]]''' Other specified congenital malformations of circulatory system
+
vertigo NOS (R42)
  
Congenital aneurysm, specified site NEC
+
*'''[[R27.0]]''' Ataxia, unspecified
  
Spinal vessel anomaly
+
''Excludes1''
  
*'''[[Q28.9]]''' Congenital malformation of circulatory system, unspecified
+
ataxia following cerebrovascular disease (I69. with final characters -93)
  
Congenital malformations of the respiratory system (Q30-Q34)
+
*'''[[R27.8]]''' Other lack of coordination
  
*'''[[Q30]]''' Congenital malformations of nose
+
*'''[[R27.9]]''' Unspecified lack of coordination
  
''Excludes1''  
+
*'''[[R29]]''' Other symptoms and signs involving the nervous and musculoskeletal systems
  
congenital deviation of nasal septum (Q67.4)
+
*'''[[R29.0]]''' Tetany
  
*'''[[Q30.0]]''' Choanal atresia
+
Carpopedal spasm
  
Atresia of nares (anterior) (posterior)
+
''Excludes1''
  
Congenital stenosis of nares (anterior) (posterior)
+
hysterical tetany (F44.5)  
  
*'''[[Q30.1]]''' Agenesis and underdevelopment of nose
+
neonatal tetany (P71.3)
  
Congenital absent of nose
+
parathyroid tetany (E20.9)
  
*'''[[Q30.2]]''' Fissured, notched and cleft nose
+
post-thyroidectomy tetany (E89.2)
  
*'''[[Q30.3]]''' Congenital perforated nasal septum
+
*'''[[R29.1]]''' Meningismus
  
*'''[[Q30.8]]''' Other congenital malformations of nose
+
*'''[[R29.2]]''' Abnormal reflex
  
Accessory nose
+
''Excludes2''
  
Congenital anomaly of nasal sinus wall
+
abnormal pupillary reflex (H57.0)
  
*'''[[Q30.9]]''' Congenital malformation of nose, unspecified
+
hyperactive gag reflex (J39.2)
  
*'''[[Q31]]''' Congenital malformations of larynx
+
vasovagal reaction or syncope (R55)
  
''Excludes1''  
+
*'''[[R29.3]]''' Abnormal posture
  
congenital laryngeal stridor NOS (P28.89)
+
*'''[[R29.4]]''' Clicking hip
  
*'''[[Q31.0]]''' Web of larynx
+
''Excludes1''  
  
Glottic web of larynx
+
congenital deformities of hip (Q65.-)
  
Subglottic web of larynx
+
*'''[[R29.5]]''' Transient paralysis ''Code first''
  
Web of larynx NOS
+
any associated spinal cord injury (S14.0, S14.1-, S24.0, S24.1-, S34.0-, S34.1-)
  
*'''[[Q31.1]]''' Congenital subglottic stenosis
+
''Excludes1''  
  
*'''[[Q31.2]]''' Laryngeal hypoplasia
+
transient ischemic attack (G45.9)
  
*'''[[Q31.3]]''' Laryngocele
+
*'''[[R29.6]]''' Repeated falls
  
*'''[[Q31.5]]''' Congenital laryngomalacia
+
Falling
  
*'''[[Q31.8]]''' Other congenital malformations of larynx
+
Tendency to fall
  
Absence of larynx
+
''Excludes2''
  
Agenesis of larynx
+
at risk for falling (Z91.81)
  
Atresia of larynx
+
history of falling (Z91.81)
  
Congenital cleft thyroid cartilage
+
*'''[[R29.7]]''' National Institutes of Health Stroke Scale (NIHSS) score ''Code first''
  
Congenital fissure of epiglottis
+
the type of cerebral infarction (I63-)
  
Congenital stenosis of larynx NEC
+
*'''[[R29.70]]''' NIHSS score 0-9
  
Posterior cleft of cricoid cartilage
+
*'''[[R29.700]]''' NIHSS score 0
  
*'''[[Q31.9]]''' Congenital malformation of larynx, unspecified
+
*'''[[R29.701]]''' NIHSS score 1
  
*'''[[Q32]]''' Congenital malformations of trachea and bronchus
+
*'''[[R29.702]]''' NIHSS score 2
  
''Excludes1''  
+
*'''[[R29.703]]''' NIHSS score 3
  
congenital bronchiectasis (Q33.4)
+
*'''[[R29.704]]''' NIHSS score 4
  
*'''[[Q32.0]]''' Congenital tracheomalacia
+
*'''[[R29.705]]''' NIHSS score 5
  
*'''[[Q32.1]]''' Other congenital malformations of trachea
+
*'''[[R29.706]]''' NIHSS score 6
  
Atresia of trachea
+
*'''[[R29.707]]''' NIHSS score 7
  
Congenital anomaly of tracheal cartilage
+
*'''[[R29.708]]''' NIHSS score 8
  
Congenital dilatation of trachea
+
*'''[[R29.709]]''' NIHSS score 9
  
Congenital malformation of trachea
+
*'''[[R29.71]]''' NIHSS score 10-19
  
Congenital stenosis of trachea
+
*'''[[R29.710]]''' NIHSS score 10
  
Congenital tracheocele
+
*'''[[R29.711]]''' NIHSS score 11
  
*'''[[Q32.2]]''' Congenital bronchomalacia
+
*'''[[R29.712]]''' NIHSS score 12
  
*'''[[Q32.3]]''' Congenital stenosis of bronchus
+
*'''[[R29.713]]''' NIHSS score 13
  
*'''[[Q32.4]]''' Other congenital malformations of bronchus
+
*'''[[R29.714]]''' NIHSS score 14
  
Absence of bronchus
+
*'''[[R29.715]]''' NIHSS score 15
  
Agenesis of bronchus
+
*'''[[R29.716]]''' NIHSS score 16
  
Atresia of bronchus
+
*'''[[R29.717]]''' NIHSS score 17
  
Congenital diverticulum of bronchus
+
*'''[[R29.718]]''' NIHSS score 18
  
Congenital malformation of bronchus NOS
+
*'''[[R29.719]]''' NIHSS score 19
  
*'''[[Q33]]''' Congenital malformations of lung
+
*'''[[R29.72]]''' NIHSS score 20-29
  
*'''[[Q33.0]]''' Congenital cystic lung
+
*'''[[R29.720]]''' NIHSS score 20
  
Congenital cystic lung disease
+
*'''[[R29.721]]''' NIHSS score 21
  
Congenital honeycomb lung
+
*'''[[R29.722]]''' NIHSS score 22
  
Congenital polycystic lung disease
+
*'''[[R29.723]]''' NIHSS score 23
  
''Excludes1''  
+
*'''[[R29.724]]''' NIHSS score 24
  
cystic fibrosis (E84.0)
+
*'''[[R29.725]]''' NIHSS score 25
  
cystic lung disease, acquired or unspecified (J98.4)
+
*'''[[R29.726]]''' NIHSS score 26
  
*'''[[Q33.1]]''' Accessory lobe of lung
+
*'''[[R29.727]]''' NIHSS score 27
  
Azygos lobe (fissured), lung
+
*'''[[R29.728]]''' NIHSS score 28
  
*'''[[Q33.2]]''' Sequestration of lung
+
*'''[[R29.729]]''' NIHSS score 29
  
*'''[[Q33.3]]''' Agenesis of lung
+
*'''[[R29.73]]''' NIHSS score 30-39
  
Congenital absence of lung (lobe)
+
*'''[[R29.730]]''' NIHSS score 30
  
*'''[[Q33.4]]''' Congenital bronchiectasis
+
*'''[[R29.731]]''' NIHSS score 31
  
*'''[[Q33.5]]''' Ectopic tissue in lung
+
*'''[[R29.732]]''' NIHSS score 32
  
*'''[[Q33.6]]''' Congenital hypoplasia and dysplasia of lung
+
*'''[[R29.733]]''' NIHSS score 33
  
''Excludes1''  
+
*'''[[R29.734]]''' NIHSS score 34
  
pulmonary hypoplasia associated with short gestation (P28.0)
+
*'''[[R29.735]]''' NIHSS score 35
  
*'''[[Q33.8]]''' Other congenital malformations of lung
+
*'''[[R29.736]]''' NIHSS score 36
  
*'''[[Q33.9]]''' Congenital malformation of lung, unspecified
+
*'''[[R29.737]]''' NIHSS score 37
  
*'''[[Q34]]''' Other congenital malformations of respiratory system
+
*'''[[R29.738]]''' NIHSS score 38
  
''Excludes2''  
+
*'''[[R29.739]]''' NIHSS score 39
  
congenital central alveolar hypoventilation syndrome (G47.35)
+
*'''[[R29.74]]''' NIHSS score 40-42
  
*'''[[Q34.0]]''' Anomaly of pleura
+
*'''[[R29.740]]''' NIHSS score 40
  
*'''[[Q34.1]]''' Congenital cyst of mediastinum
+
*'''[[R29.741]]''' NIHSS score 41
  
*'''[[Q34.8]]''' Other specified congenital malformations of respiratory system
+
*'''[[R29.742]]''' NIHSS score 42
  
Atresia of nasopharynx
+
*'''[[R29.8]]''' Other symptoms and signs involving the nervous and musculoskeletal systems
  
*'''[[Q34.9]]''' Congenital malformation of respiratory system, unspecified
+
*'''[[R29.81]]''' Other symptoms and signs involving the nervous system
  
Congenital absence of respiratory system
+
*'''[[R29.810]]''' Facial weakness
  
Congenital anomaly of respiratory system NOS
+
Facial droop
  
Cleft lip and cleft palate (Q35-Q37) ''Use additional''  
+
''Excludes1''  
  
code to identify associated malformation of the nose (Q30.2)  
+
Bell's palsy (G51.0)  
  
''Excludes1''
+
facial weakness following cerebrovascular disease (I69. with final characters -92)
  
Robin's syndrome (Q87.0)
+
*'''[[R29.818]]''' Other symptoms and signs involving the nervous system
  
*'''[[Q35]]''' Cleft palate
+
*'''[[R29.89]]''' Other symptoms and signs involving the musculoskeletal system
  
''Includes''  
+
''Excludes2''  
  
fissure of palate
+
pain in limb (M79.6-)
  
palatoschisis
+
*'''[[R29.890]]''' Loss of height
  
 
''Excludes1''  
 
''Excludes1''  
  
cleft palate with cleft lip (Q37.-)
+
osteoporosis (M80-M81)
 +
 
 +
*'''[[R29.891]]''' Ocular torticollis
  
*'''[[Q35.1]]''' Cleft hard palate
+
''Excludes1''  
  
*'''[[Q35.3]]''' Cleft soft palate
+
congenital (sternomastoid) torticollis Q68.0
  
*'''[[Q35.5]]''' Cleft hard palate with cleft soft palate
+
psychogenic torticollis (F45.8)
  
*'''[[Q35.7]]''' Cleft uvula
+
spasmodic torticollis (G24.3)
  
*'''[[Q35.9]]''' Cleft palate, unspecified
+
torticollis due to birth injury (P15.8)
  
Cleft palate NOS
+
torticollis NOS M43.6
  
*'''[[Q36]]''' Cleft lip
+
*'''[[R29.898]]''' Other symptoms and signs involving the musculoskeletal system
  
''Includes''  
+
*'''[[R29.9]]''' Unspecified symptoms and signs involving the nervous and musculoskeletal systems
  
cheiloschisis
+
*'''[[R29.90]]''' Unspecified symptoms and signs involving the nervous system
  
congenital fissure of lip
+
*'''[[R29.91]]''' Unspecified symptoms and signs involving the musculoskeletal system
  
harelip
+
Symptoms and signs involving the genitourinary system (R30-R39)
  
labium leporinum
+
*'''[[R30]]''' Pain associated with micturition
  
 
''Excludes1''  
 
''Excludes1''  
  
cleft lip with cleft palate (Q37.-)
+
psychogenic pain associated with micturition (F45.8)
  
*'''[[Q36.0]]''' Cleft lip, bilateral
+
*'''[[R30.0]]''' Dysuria
  
*'''[[Q36.1]]''' Cleft lip, median
+
Strangury
  
*'''[[Q36.9]]''' Cleft lip, unilateral
+
*'''[[R30.1]]''' Vesical tenesmus
  
Cleft lip NOS
+
*'''[[R30.9]]''' Painful micturition, unspecified
  
*'''[[Q37]]''' Cleft palate with cleft lip
+
Painful urination NOS
  
''Includes''  
+
*'''[[R31]]''' Hematuria
  
cheilopalatoschisis
+
''Excludes1''
  
*'''[[Q37.0]]''' Cleft hard palate with bilateral cleft lip
+
hematuria included with underlying conditions, such as
  
*'''[[Q37.1]]''' Cleft hard palate with unilateral cleft lip
+
acute cystitis with hematuria (N30.01)
  
Cleft hard palate with cleft lip NOS
+
recurrent and persistent hematuria in glomerular diseases (N02.-)
  
*'''[[Q37.2]]''' Cleft soft palate with bilateral cleft lip
+
*'''[[R31.0]]''' Gross hematuria
  
*'''[[Q37.3]]''' Cleft soft palate with unilateral cleft lip
+
*'''[[R31.1]]''' Benign essential microscopic hematuria
  
Cleft soft palate with cleft lip NOS
+
*'''[[R31.2]]''' Other microscopic hematuria
  
*'''[[Q37.4]]''' Cleft hard and soft palate with bilateral cleft lip
+
*'''[[R31.21]]''' Asymptomatic microscopic hematuria
  
*'''[[Q37.5]]''' Cleft hard and soft palate with unilateral cleft lip
+
AMH
  
Cleft hard and soft palate with cleft lip NOS
+
*'''[[R31.29]]''' Other microscopic hematuria
  
*'''[[Q37.8]]''' Unspecified cleft palate with bilateral cleft lip
+
*'''[[R31.9]]''' Hematuria, unspecified
  
*'''[[Q37.9]]''' Unspecified cleft palate with unilateral cleft lip
+
*'''[[R32]]''' Unspecified urinary incontinence
  
Cleft palate with cleft lip NOS
+
Enuresis NOS  
  
Other congenital malformations of the digestive system (Q38-Q45)
+
''Excludes1''
  
*'''[[Q38]]''' Other congenital malformations of tongue, mouth and pharynx
+
functional urinary incontinence (R39.81)
  
''Excludes1''
+
nonorganic enuresis (F98.0)
  
dentofacial anomalies (M26.-)  
+
stress incontinence and other specified urinary incontinence (N39.3-N39.4-)  
  
macrostomia (Q18.4)  
+
urinary incontinence associated with cognitive impairment (R39.81)
  
microstomia (Q18.5)
+
*'''[[R33]]''' Retention of urine
  
*'''[[Q38.0]]''' Congenital malformations of lips, not elsewhere classified
+
''Excludes1''  
  
Congenital fistula of lip
+
psychogenic retention of urine (F45.8)
  
Congenital malformation of lip NOS
+
*'''[[R33.0]]''' Drug induced retention of urine ''Use additional''
  
Van der Woude's syndrome
+
code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
  
''Excludes1''  
+
*'''[[R33.8]]''' Other retention of urine ''Code first''
  
cleft lip (Q36.-)
+
, if applicable, any causal condition, such as
  
cleft lip with cleft palate (Q37.-)  
+
enlarged prostate (N40.1)
  
macrocheilia (Q18.6)
+
*'''[[R33.9]]''' Retention of urine, unspecified
  
microcheilia (Q18.7)
+
*'''[[R34]]''' Anuria and oliguria
  
*'''[[Q38.1]]''' Ankyloglossia
+
''Excludes1''  
  
Tongue tie
+
anuria and oliguria complicating abortion or ectopic or molar pregnancy (O00-O07, O08.4)
  
*'''[[Q38.2]]''' Macroglossia
+
anuria and oliguria complicating pregnancy (O26.83-)
  
Congenital hypertrophy of tongue
+
anuria and oliguria complicating the puerperium (O90.4)
  
*'''[[Q38.3]]''' Other congenital malformations of tongue
+
*'''[[R35]]''' Polyuria ''Code first''
  
Aglossia
+
, if applicable, any causal condition, such as
  
Bifid tongue
+
enlarged prostate (N40.1)
  
Congenital adhesion of tongue
+
''Excludes1''
  
Congenital fissure of tongue
+
psychogenic polyuria (F45.8)
  
Congenital malformation of tongue NOS
+
*'''[[R35.0]]''' Frequency of micturition
  
Double tongue
+
*'''[[R35.1]]''' Nocturia
  
Hypoglossia
+
*'''[[R35.8]]''' Other polyuria
  
Hypoplasia of tongue
+
Polyuria NOS
  
Microglossia
+
*'''[[R36]]''' Urethral discharge
  
*'''[[Q38.4]]''' Congenital malformations of salivary glands and ducts
+
*'''[[R36.0]]''' Urethral discharge without blood
  
Atresia of salivary glands and ducts
+
*'''[[R36.1]]''' Hematospermia
  
Congenital absence of salivary glands and ducts
+
*'''[[R36.9]]''' Urethral discharge, unspecified
  
Congenital accessory salivary glands and ducts
+
Penile discharge NOS
  
Congenital fistula of salivary gland
+
Urethrorrhea
  
*'''[[Q38.5]]''' Congenital malformations of palate, not elsewhere classified
+
*'''[[R37]]''' Sexual dysfunction, unspecified
  
Congenital absence of uvula
+
*'''[[R39]]''' Other and unspecified symptoms and signs involving the genitourinary system
  
Congenital malformation of palate NOS
+
*'''[[R39.0]]''' Extravasation of urine
  
Congenital high arched palate
+
*'''[[R39.1]]''' Other difficulties with micturition ''Code first''
  
''Excludes1''
+
, if applicable, any causal condition, such as
 +
 
 +
enlarged prostate (N40.1)
  
cleft palate (Q35.-)
+
*'''[[R39.11]]''' Hesitancy of micturition
  
cleft palate with cleft lip (Q37.-)
+
*'''[[R39.12]]''' Poor urinary stream
  
*'''[[Q38.6]]''' Other congenital malformations of mouth
+
Weak urinary steam
  
Congenital malformation of mouth NOS
+
*'''[[R39.13]]''' Splitting of urinary stream
  
*'''[[Q38.7]]''' Congenital pharyngeal pouch
+
*'''[[R39.14]]''' Feeling of incomplete bladder emptying
  
Congenital diverticulum of pharynx
+
*'''[[R39.15]]''' Urgency of urination
  
 
''Excludes1''  
 
''Excludes1''  
  
pharyngeal pouch syndrome (D82.1)
+
urge incontinence (N39.41, N39.46)
 +
 
 +
*'''[[R39.16]]''' Straining to void
  
*'''[[Q38.8]]''' Other congenital malformations of pharynx
+
*'''[[R39.19]]''' Other difficulties with micturition
  
Congenital malformation of pharynx NOS
+
*'''[[R39.191]]''' Need to immediately re-void
  
Imperforate pharynx
+
*'''[[R39.192]]''' Position dependent micturition
  
*'''[[Q39]]''' Congenital malformations of esophagus
+
*'''[[R39.198]]''' Other difficulties with micturition
  
*'''[[Q39.0]]''' Atresia of esophagus without fistula
+
*'''[[R39.2]]''' Extrarenal uremia
  
Atresia of esophagus NOS
+
Prerenal uremia
  
*'''[[Q39.1]]''' Atresia of esophagus with tracheo-esophageal fistula
+
''Excludes1''  
  
Atresia of esophagus with broncho-esophageal fistula
+
uremia NOS (N19)
  
*'''[[Q39.2]]''' Congenital tracheo-esophageal fistula without atresia
+
*'''[[R39.8]]''' Other symptoms and signs involving the genitourinary system
  
Congenital tracheo-esophageal fistula NOS
+
*'''[[R39.81]]''' Functional urinary incontinence
  
*'''[[Q39.3]]''' Congenital stenosis and stricture of esophagus
+
Urinary incontinence due to cognitive impairment, or severe physical disability or immobility
  
*'''[[Q39.4]]''' Esophageal web
+
''Excludes1''  
  
*'''[[Q39.5]]''' Congenital dilatation of esophagus
+
stress incontinence and other specified urinary incontinence (N39.3-N39.4-)
  
Congenital cardiospasm
+
urinary incontinence NOS (R32)
  
*'''[[Q39.6]]''' Congenital diverticulum of esophagus
+
*'''[[R39.82]]''' Chronic bladder pain
  
Congenital esophageal pouch
+
*'''[[R39.83]]''' Unilateral non-palpable testicle
  
*'''[[Q39.8]]''' Other congenital malformations of esophagus
+
*'''[[R39.84]]''' Bilateral non-palpable testicles
  
Congenital absence of esophagus
+
*'''[[R39.89]]''' Other symptoms and signs involving the genitourinary system
  
Congenital displacement of esophagus
+
*'''[[R39.9]]''' Unspecified symptoms and signs involving the genitourinary system
  
Congenital duplication of esophagus
+
Symptoms and signs involving cognition, perception, emotional state and behavior (R40-R46)
  
*'''[[Q39.9]]''' Congenital malformation of esophagus, unspecified
+
''Excludes2''  
  
*'''[[Q40]]''' Other congenital malformations of upper alimentary tract
+
symptoms and signs constituting part of a pattern of mental disorder (F01-F99)
  
*'''[[Q40.0]]''' Congenital hypertrophic pyloric stenosis
+
*'''[[R40]]''' Somnolence, stupor and coma
  
Congenital or infantile constriction
+
''Excludes1''
  
Congenital or infantile hypertrophy
+
neonatal coma (P91.5)
  
Congenital or infantile spasm
+
somnolence, stupor and coma in diabetes (E08-E13)
  
Congenital or infantile stenosis
+
somnolence, stupor and coma in hepatic failure (K72.-)
  
Congenital or infantile stricture
+
somnolence, stupor and coma in hypoglycemia (nondiabetic) (E15)
  
*'''[[Q40.1]]''' Congenital hiatus hernia
+
*'''[[R40.0]]''' Somnolence
  
Congenital displacement of cardia through esophageal hiatus
+
Drowsiness
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital diaphragmatic hernia (Q79.0)
+
coma (R40.2-)
 +
 
 +
*'''[[R40.1]]''' Stupor
 +
 
 +
Catatonic stupor
 +
 
 +
Semicoma
  
*'''[[Q40.2]]''' Other specified congenital malformations of stomach
+
''Excludes1''  
  
Congenital displacement of stomach
+
catatonic schizophrenia (F20.2)
  
Congenital diverticulum of stomach
+
coma (R40.2-)
  
Congenital hourglass stomach
+
depressive stupor (F31-F33)
  
Congenital duplication of stomach
+
dissociative stupor (F44.2)
  
Megalogastria
+
manic stupor (F30.2)
  
Microgastria
+
*'''[[R40.2]]''' Coma ''Code first''
  
*'''[[Q40.3]]''' Congenital malformation of stomach, unspecified
+
any associated
  
*'''[[Q40.8]]''' Other specified congenital malformations of upper alimentary tract
+
fracture of skull (S02.-)
  
*'''[[Q40.9]]''' Congenital malformation of upper alimentary tract, unspecified
+
intracranial injury (S06.-)
  
Congenital anomaly of upper alimentary tract
+
Note
  
Congenital deformity of upper alimentary tract
+
One code from each subcategory, R40.21-R40.23, is required to complete the coma scale
  
*'''[[Q41]]''' Congenital absence, atresia and stenosis of small intestine
+
*'''[[R40.20]]''' Unspecified coma
  
''Includes''
+
Coma NOS
  
congenital obstruction, occlusion or stricture of small intestine or intestine NOS  
+
Unconsciousness NOS
  
''Excludes1''  
+
*'''[[R40.21]]''' Coma scale, eyes open
  
cystic fibrosis with intestinal manifestation (E84.11)
+
The following appropriate 7th character is to be added to subcategory R40.21-
  
meconium ileus NOS (without cystic fibrosis) (P76.0)
+
0 - unspecified time
  
*'''[[Q41.0]]''' Congenital absence, atresia and stenosis of duodenum
+
1 - in the field (EMT or ambulance)
  
*'''[[Q41.1]]''' Congenital absence, atresia and stenosis of jejunum
+
2 - at arrival to emergency department
  
Apple peel syndrome
+
3 - at hospital admission
  
Imperforate jejunum
+
4 - 24 hours or more after hospital admission
  
*'''[[Q41.2]]''' Congenital absence, atresia and stenosis of ileum
+
*'''[[R40.211]]''' Coma scale, eyes open, never
  
*'''[[Q41.8]]''' Congenital absence, atresia and stenosis of other specified parts of small intestine
+
Coma scale eye opening score of 1
  
*'''[[Q41.9]]''' Congenital absence, atresia and stenosis of small intestine, part unspecified
+
*'''[[R40.212]]''' Coma scale, eyes open, to pain
  
Congenital absence, atresia and stenosis of intestine NOS
+
Coma scale eye opening score of 2
  
*'''[[Q42]]''' Congenital absence, atresia and stenosis of large intestine
+
*'''[[R40.213]]''' Coma scale, eyes open, to sound
  
''Includes''
+
Coma scale eye opening score of 3
  
congenital obstruction, occlusion and stricture of large intestine
+
*'''[[R40.214]]''' Coma scale, eyes open, spontaneous
  
*'''[[Q42.0]]''' Congenital absence, atresia and stenosis of rectum with fistula
+
Coma scale eye opening score of 4
  
*'''[[Q42.1]]''' Congenital absence, atresia and stenosis of rectum without fistula
+
*'''[[R40.22]]''' Coma scale, best verbal response
  
Imperforate rectum
+
The following appropriate 7th character is to be added to subcategory R40.22-
  
*'''[[Q42.2]]''' Congenital absence, atresia and stenosis of anus with fistula
+
0 - unspecified time
  
*'''[[Q42.3]]''' Congenital absence, atresia and stenosis of anus without fistula
+
1 - in the field (EMT or ambulance)
  
Imperforate anus
+
2 - at arrival to emergency department
  
*'''[[Q42.8]]''' Congenital absence, atresia and stenosis of other parts of large intestine
+
3 - at hospital admission
  
*'''[[Q42.9]]''' Congenital absence, atresia and stenosis of large intestine, part unspecified
+
4 - 24 hours or more after hospital admission
  
*'''[[Q43]]''' Other congenital malformations of intestine
+
*'''[[R40.221]]''' Coma scale, best verbal response, none
  
*'''[[Q43.0]]''' Meckel's diverticulum (displaced) (hypertrophic)
+
Coma scale verbal score of 1
  
Persistent omphalomesenteric duct
+
*'''[[R40.222]]''' Coma scale, best verbal response, incomprehensible words
  
Persistent vitelline duct
+
Coma scale verbal score of 2
  
*'''[[Q43.1]]''' Hirschsprung's disease
+
Incomprehensible sounds (2-5 years of age)
  
Aganglionosis
+
Moans/grunts to pain; restless (<2 years old)
  
Congenital (aganglionic) megacolon
+
*'''[[R40.223]]''' Coma scale, best verbal response, inappropriate words
  
*'''[[Q43.2]]''' Other congenital functional disorders of colon
+
Coma scale verbal score of 3
  
Congenital dilatation of colon
+
Inappropriate crying or screaming (< 2 years of age)
  
*'''[[Q43.3]]''' Congenital malformations of intestinal fixation
+
Screaming (2-5 years of age)
  
Congenital omental, anomalous adhesions (bands)
+
*'''[[R40.224]]''' Coma scale, best verbal response, confused conversation
  
Congenital peritoneal adhesions (bands)
+
Coma scale verbal score of 4
  
Incomplete rotation of cecum and colon
+
Inappropriate words (2-5 years of age)
  
Insufficient rotation of cecum and colon
+
Irritable cries (< 2 years of age)
  
Jackson's membrane
+
*'''[[R40.225]]''' Coma scale, best verbal response, oriented
  
Malrotation of colon
+
Coma scale verbal score of 5
  
Rotation failure of cecum and colon
+
Cooing or babbling or crying appropriately (< 2 years of age)
  
Universal mesentery
+
Uses appropriate words (2- 5 years of age)
  
*'''[[Q43.4]]''' Duplication of intestine
+
*'''[[R40.23]]''' Coma scale, best motor response
  
*'''[[Q43.5]]''' Ectopic anus
+
The following appropriate 7th character is to be added to subcategory R40.23-
  
*'''[[Q43.6]]''' Congenital fistula of rectum and anus
+
0 - unspecified time
  
''Excludes1''
+
1 - in the field (EMT or ambulance)
  
congenital fistula of anus with absence, atresia and stenosis (Q42.2)
+
2 - at arrival to emergency department
  
congenital fistula of rectum with absence, atresia and stenosis (Q42.0)
+
3 - at hospital admission
  
congenital rectovaginal fistula (Q52.2)
+
4 - 24 hours or more after hospital admission
  
congenital urethrorectal fistula (Q64.73)
+
*'''[[R40.231]]''' Coma scale, best motor response, none
  
pilonidal fistula or sinus (L05.-)
+
Coma scale motor score of 1
  
*'''[[Q43.7]]''' Persistent cloaca
+
*'''[[R40.232]]''' Coma scale, best motor response, extension
  
Cloaca NOS
+
Abnormal extensor posturing to pain or noxious stimuli (< 2 years of age)
  
*'''[[Q43.8]]''' Other specified congenital malformations of intestine
+
Coma scale motor score of 2
  
Congenital blind loop syndrome
+
Extensor posturing to pain or noxious stimuli (2-5 years of age)
  
Congenital diverticulitis, colon
+
*'''[[R40.233]]''' Coma scale, best motor response, abnormal flexion
  
Congenital diverticulum, intestine
+
Abnormal flexure posturing to pain or noxious stimuli (2-5 years of age)
  
Dolichocolon
+
Coma scale motor score of 3
  
Megaloappendix
+
Flexion/decorticate posturing (< 2 years of age)
  
Megaloduodenum
+
*'''[[R40.234]]''' Coma scale, best motor response, flexion withdrawal
  
Microcolon
+
Coma scale motor score of 4
  
Transposition of appendix
+
Withdraws from pain or noxious stimuli (2-5 years of age)
  
Transposition of colon
+
*'''[[R40.235]]''' Coma scale, best motor response, localizes pain
  
Transposition of intestine
+
Coma scale motor score of 5
  
*'''[[Q43.9]]''' Congenital malformation of intestine, unspecified
+
Localizes pain (2-5 years of age)
  
*'''[[Q44]]''' Congenital malformations of gallbladder, bile ducts and liver
+
Withdraws to touch (< 2 years of age)
  
*'''[[Q44.0]]''' Agenesis, aplasia and hypoplasia of gallbladder
+
*'''[[R40.236]]''' Coma scale, best motor response, obeys commands
  
Congenital absence of gallbladder
+
Coma scale motor score of 6
  
*'''[[Q44.1]]''' Other congenital malformations of gallbladder
+
Normal or spontaneous movement (< 2 years of age)
  
Congenital malformation of gallbladder NOS
+
Obeys commands (2-5 years of age)
  
Intrahepatic gallbladder
+
*'''[[R40.24]]''' Glasgow coma scale, total score
  
*'''[[Q44.2]]''' Atresia of bile ducts
+
Note
  
*'''[[Q44.3]]''' Congenital stenosis and stricture of bile ducts
+
Assign a code from subcategory R40.24, when only the total coma score is documented
  
*'''[[Q44.4]]''' Choledochal cyst
+
The following appropriate 7th character is to be added to subcategory R40.24-
  
*'''[[Q44.5]]''' Other congenital malformations of bile ducts
+
0 - unspecified time
  
Accessory hepatic duct
+
1 - in the field (EMT or ambulance)
  
Biliary duct duplication
+
2 - at arrival to emergency department
  
Congenital malformation of bile duct NOS
+
3 - at hospital admission
  
Cystic duct duplication
+
4 - 24 hours or more after hospital admission
  
*'''[[Q44.6]]''' Cystic disease of liver
+
*'''[[R40.241]]''' Glasgow coma scale score 13-15
  
Fibrocystic disease of liver
+
*'''[[R40.242]]''' Glasgow coma scale score 9-12
  
*'''[[Q44.7]]''' Other congenital malformations of liver
+
*'''[[R40.243]]''' Glasgow coma scale score 3-8
  
Accessory liver
+
*'''[[R40.244]]''' Other coma, without documented Glasgow coma scale score, or with partial score
  
Alagille's syndrome
+
reported
  
Congenital absence of liver
+
*'''[[R40.3]]''' Persistent vegetative state
  
Congenital hepatomegaly
+
*'''[[R40.4]]''' Transient alteration of awareness
  
Congenital malformation of liver NOS
+
*'''[[R41]]''' Other symptoms and signs involving cognitive functions and awareness
  
*'''[[Q45]]''' Other congenital malformations of digestive system
+
''Excludes1''  
  
''Excludes2''
+
dissociative (conversion) disorders (F44.-)
  
congenital diaphragmatic hernia (Q79.0)  
+
mild cognitive impairment, so stated (G31.84)
  
congenital hiatus hernia (Q40.1)
+
*'''[[R41.0]]''' Disorientation, unspecified
  
*'''[[Q45.0]]''' Agenesis, aplasia and hypoplasia of pancreas
+
Confusion NOS
  
Congenital absence of pancreas
+
Delirium NOS
  
*'''[[Q45.1]]''' Annular pancreas
+
*'''[[R41.1]]''' Anterograde amnesia
  
*'''[[Q45.2]]''' Congenital pancreatic cyst
+
*'''[[R41.2]]''' Retrograde amnesia
  
*'''[[Q45.3]]''' Other congenital malformations of pancreas and pancreatic duct
+
*'''[[R41.3]]''' Other amnesia
  
Accessory pancreas
+
Amnesia NOS
  
Congenital malformation of pancreas or pancreatic duct NOS  
+
Memory loss NOS  
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital diabetes mellitus (E10.-)  
+
amnestic disorder due to known physiologic condition (F04)  
  
cystic fibrosis (E84.0-E84.9)  
+
amnestic syndrome due to psychoactive substance use (F10-F19 with 5th character .6)  
  
fibrocystic disease of pancreas (E84.-)  
+
mild memory disturbance due to known physiological condition (F06.8)  
  
neonatal diabetes mellitus (P70.2)
+
transient global amnesia (G45.4)
  
*'''[[Q45.8]]''' Other specified congenital malformations of digestive system
+
*'''[[R41.4]]''' Neurologic neglect syndrome
  
Absence (complete) (partial) of alimentary tract NOS
+
Asomatognosia
  
Duplication of digestive system
+
Hemi-akinesia
  
Malposition, congenital of digestive system
+
Hemi-inattention
  
*'''[[Q45.9]]''' Congenital malformation of digestive system, unspecified
+
Hemispatial neglect
  
Congenital anomaly of digestive system
+
Left-sided neglect
  
Congenital deformity of digestive system
+
Sensory neglect
  
Congenital malformations of genital organs (Q50-Q56)
+
Visuospatial neglect
  
 
''Excludes1''  
 
''Excludes1''  
  
androgen insensitivity syndrome (E34.5-)  
+
visuospatial deficit (R41.842)
  
syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)
+
*'''[[R41.8]]''' Other symptoms and signs involving cognitive functions and awareness
  
*'''[[Q50]]''' Congenital malformations of ovaries, fallopian tubes and broad ligaments
+
*'''[[R41.81]]''' Age-related cognitive decline
  
*'''[[Q50.0]]''' Congenital absence of ovary
+
Senility NOS
  
''Excludes1''
+
*'''[[R41.82]]''' Altered mental status, unspecified
  
Turner's syndrome (Q96.-)
+
Change in mental status NOS
  
*'''[[Q50.01]]''' Congenital absence of ovary, unilateral
+
''Excludes1''  
  
*'''[[Q50.02]]''' Congenital absence of ovary, bilateral
+
altered level of consciousness (R40.-)
  
*'''[[Q50.1]]''' Developmental ovarian cyst
+
altered mental status due to known condition - code to condition
  
*'''[[Q50.2]]''' Congenital torsion of ovary
+
delirium NOS (R41.0)
  
*'''[[Q50.3]]''' Other congenital malformations of ovary
+
*'''[[R41.83]]''' Borderline intellectual functioning
  
*'''[[Q50.31]]''' Accessory ovary
+
IQ level 71 to 84
  
*'''[[Q50.32]]''' Ovarian streak
+
''Excludes1''  
  
46, XX with streak gonads
+
intellectual disabilities (F70-F79)
  
*'''[[Q50.39]]''' Other congenital malformation of ovary
+
*'''[[R41.84]]''' Other specified cognitive deficit
  
Congenital malformation of ovary NOS
+
''Excludes1''
  
*'''[[Q50.4]]''' Embryonic cyst of fallopian tube
+
cognitive deficits as sequelae of cerebrovascular disease (I69.01-, I69.11-, I69.21-, I69.31-
  
Fimbrial cyst
+
, I69.81-, I69.91-)
  
*'''[[Q50.5]]''' Embryonic cyst of broad ligament
+
*'''[[R41.840]]''' Attention and concentration deficit
  
Epoophoron cyst
+
''Excludes1''
  
Parovarian cyst
+
attention-deficit hyperactivity disorders (F90.-)
  
*'''[[Q50.6]]''' Other congenital malformations of fallopian tube and broad ligament
+
*'''[[R41.841]]''' Cognitive communication deficit
  
Absence of fallopian tube and broad ligament
+
*'''[[R41.842]]''' Visuospatial deficit
  
Accessory fallopian tube and broad ligament
+
*'''[[R41.843]]''' Psychomotor deficit
  
Atresia of fallopian tube and broad ligament
+
*'''[[R41.844]]''' Frontal lobe and executive function deficit
  
Congenital malformation of fallopian tube or broad ligament NOS
+
*'''[[R41.89]]''' Other symptoms and signs involving cognitive functions and awareness
  
*'''[[Q51]]''' Congenital malformations of uterus and cervix
+
Anosognosia
  
*'''[[Q51.0]]''' Agenesis and aplasia of uterus
+
*'''[[R41.9]]''' Unspecified symptoms and signs involving cognitive functions and awareness
  
Congenital absence of uterus
+
Unspecified neurocognitive disorder
  
*'''[[Q51.1]]''' Doubling of uterus with doubling of cervix and vagina
+
*'''[[R42]]''' Dizziness and giddiness
  
*'''[[Q51.10]]''' Doubling of uterus with doubling of cervix and vagina without obstruction
+
Light-headedness
  
Doubling of uterus with doubling of cervix and vagina NOS
+
Vertigo NOS  
  
*'''[[Q51.11]]''' Doubling of uterus with doubling of cervix and vagina with obstruction
+
''Excludes1''  
  
*'''[[Q51.2]]''' Other doubling of uterus
+
vertiginous syndromes (H81.-)
  
Doubling of uterus NOS
+
vertigo from infrasound (T75.23)
  
Septate uterus
+
*'''[[R43]]''' Disturbances of smell and taste
  
*'''[[Q51.20]]''' Other doubling of uterus, unspecified
+
*'''[[R43.0]]''' Anosmia
  
Septate uterus, unspecified
+
*'''[[R43.1]]''' Parosmia
  
*'''[[Q51.21]]''' Other complete doubling of uterus
+
*'''[[R43.2]]''' Parageusia
  
Complete septate uterus
+
*'''[[R43.8]]''' Other disturbances of smell and taste
  
*'''[[Q51.22]]''' Other partial doubling of uterus
+
Mixed disturbance of smell and taste
  
Partial septate uterus
+
*'''[[R43.9]]''' Unspecified disturbances of smell and taste
  
*'''[[Q51.28]]''' Other doubling of uterus, other specified
+
*'''[[R44]]''' Other symptoms and signs involving general sensations and perceptions
  
Septate uterus, other specified
+
''Excludes1''
  
*'''[[Q51.3]]''' Bicornate uterus
+
alcoholic hallucinations (F1.5)
  
Bicornate uterus, complete or partial
+
hallucinations in drug psychosis (F11-F19 with .5)
  
*'''[[Q51.4]]''' Unicornate uterus
+
hallucinations in mood disorders with psychotic symptoms (F30.2, F31.5, F32.3, F33.3)
  
Unicornate uterus with or without a separate uterine horn
+
hallucinations in schizophrenia, schizotypal and delusional disorders (F20-F29)
  
Uterus with only one functioning horn
+
''Excludes2''
  
*'''[[Q51.5]]''' Agenesis and aplasia of cervix
+
disturbances of skin sensation (R20.-)
  
Congenital absence of cervix
+
*'''[[R44.0]]''' Auditory hallucinations
  
*'''[[Q51.6]]''' Embryonic cyst of cervix
+
*'''[[R44.1]]''' Visual hallucinations
  
*'''[[Q51.7]]''' Congenital fistulae between uterus and digestive and urinary tracts
+
*'''[[R44.2]]''' Other hallucinations
  
*'''[[Q51.8]]''' Other congenital malformations of uterus and cervix
+
*'''[[R44.3]]''' Hallucinations, unspecified
  
*'''[[Q51.81]]''' Other congenital malformations of uterus
+
*'''[[R44.8]]''' Other symptoms and signs involving general sensations and perceptions
  
*'''[[Q51.810]]''' Arcuate uterus
+
*'''[[R44.9]]''' Unspecified symptoms and signs involving general sensations and perceptions
  
Arcuatus uterus
+
*'''[[R45]]''' Symptoms and signs involving emotional state
  
*'''[[Q51.811]]''' Hypoplasia of uterus
+
*'''[[R45.0]]''' Nervousness
  
*'''[[Q51.818]]''' Other congenital malformations of uterus
+
Nervous tension
  
Müllerian anomaly of uterus NEC
+
*'''[[R45.1]]''' Restlessness and agitation
  
*'''[[Q51.82]]''' Other congenital malformations of cervix
+
*'''[[R45.2]]''' Unhappiness
  
*'''[[Q51.820]]''' Cervical duplication
+
*'''[[R45.3]]''' Demoralization and apathy
  
*'''[[Q51.821]]''' Hypoplasia of cervix
+
''Excludes1''  
  
*'''[[Q51.828]]''' Other congenital malformations of cervix
+
anhedonia (R45.84)
  
*'''[[Q51.9]]''' Congenital malformation of uterus and cervix, unspecified
+
*'''[[R45.4]]''' Irritability and anger
  
*'''[[Q52]]''' Other congenital malformations of female genitalia
+
*'''[[R45.5]]''' Hostility
  
*'''[[Q52.0]]''' Congenital absence of vagina
+
*'''[[R45.6]]''' Violent behavior
  
Vaginal agenesis, total or partial
+
*'''[[R45.7]]''' State of emotional shock and stress, unspecified
  
*'''[[Q52.1]]''' Doubling of vagina
+
*'''[[R45.8]]''' Other symptoms and signs involving emotional state
  
''Excludes1''  
+
*'''[[R45.81]]''' Low self-esteem
  
doubling of vagina with doubling of uterus and cervix (Q51.1-)
+
*'''[[R45.82]]''' Worries
  
*'''[[Q52.10]]''' Doubling of vagina, unspecified
+
*'''[[R45.83]]''' Excessive crying of child, adolescent or adult
  
Septate vagina NOS
+
''Excludes1''
  
*'''[[Q52.11]]''' Transverse vaginal septum
+
excessive crying of infant (baby) R68.11
  
*'''[[Q52.12]]''' Longitudinal vaginal septum
+
*'''[[R45.84]]''' Anhedonia
  
*'''[[Q52.120]]''' Longitudinal vaginal septum, nonobstructing
+
*'''[[R45.85]]''' Homicidal and suicidal ideations
  
*'''[[Q52.121]]''' Longitudinal vaginal septum, obstructing, right side
+
''Excludes1''  
  
*'''[[Q52.122]]''' Longitudinal vaginal septum, obstructing, left side
+
suicide attempt (T14.91)
  
*'''[[Q52.123]]''' Longitudinal vaginal septum, microperforate, right side
+
*'''[[R45.850]]''' Homicidal ideations
  
*'''[[Q52.124]]''' Longitudinal vaginal septum, microperforate, left side
+
*'''[[R45.851]]''' Suicidal ideations
  
*'''[[Q52.129]]''' Other and unspecified longitudinal vaginal septum
+
*'''[[R45.86]]''' Emotional lability
  
*'''[[Q52.2]]''' Congenital rectovaginal fistula
+
*'''[[R45.87]]''' Impulsiveness
  
''Excludes1''  
+
*'''[[R45.89]]''' Other symptoms and signs involving emotional state
  
cloaca (Q43.7)
+
*'''[[R46]]''' Symptoms and signs involving appearance and behavior
  
*'''[[Q52.3]]''' Imperforate hymen
+
''Excludes1''  
  
*'''[[Q52.4]]''' Other congenital malformations of vagina
+
appearance and behavior in schizophrenia, schizotypal and delusional disorders (F20-F29)
  
Canal of Nuck cyst, congenital
+
mental and behavioral disorders (F01-F99)
  
Congenital malformation of vagina NOS
+
*'''[[R46.0]]''' Very low level of personal hygiene
  
Embryonic vaginal cyst
+
*'''[[R46.1]]''' Bizarre personal appearance
  
Gartner's duct cyst
+
*'''[[R46.2]]''' Strange and inexplicable behavior
  
*'''[[Q52.5]]''' Fusion of labia
+
*'''[[R46.3]]''' Overactivity
  
*'''[[Q52.6]]''' Congenital malformation of clitoris
+
*'''[[R46.4]]''' Slowness and poor responsiveness
  
*'''[[Q52.7]]''' Other and unspecified congenital malformations of vulva
+
''Excludes1''  
  
*'''[[Q52.70]]''' Unspecified congenital malformations of vulva
+
stupor (R40.1)
  
Congenital malformation of vulva NOS
+
*'''[[R46.5]]''' Suspiciousness and marked evasiveness
  
*'''[[Q52.71]]''' Congenital absence of vulva
+
*'''[[R46.6]]''' Undue concern and preoccupation with stressful events
  
*'''[[Q52.79]]''' Other congenital malformations of vulva
+
*'''[[R46.7]]''' Verbosity and circumstantial detail obscuring reason for contact
  
Congenital cyst of vulva
+
*'''[[R46.8]]''' Other symptoms and signs involving appearance and behavior
  
*'''[[Q52.8]]''' Other specified congenital malformations of female genitalia
+
*'''[[R46.81]]''' Obsessive-compulsive behavior
  
*'''[[Q52.9]]''' Congenital malformation of female genitalia, unspecified
+
''Excludes1''  
  
*'''[[Q53]]''' Undescended and ectopic testicle
+
obsessive-compulsive disorder (F42-)
  
*'''[[Q53.0]]''' Ectopic testis
+
*'''[[R46.89]]''' Other symptoms and signs involving appearance and behavior
  
*'''[[Q53.00]]''' Ectopic testis, unspecified
+
Symptoms and signs involving speech and voice (R47-R49)
  
*'''[[Q53.01]]''' Ectopic testis, unilateral
+
*'''[[R47]]''' Speech disturbances, not elsewhere classified
  
*'''[[Q53.02]]''' Ectopic testes, bilateral
+
''Excludes1''  
  
*'''[[Q53.1]]''' Undescended testicle, unilateral
+
autism (F84.0)
  
*'''[[Q53.10]]''' Unspecified undescended testicle, unilateral
+
cluttering (F80.81)
  
*'''[[Q53.11]]''' Abdominal testis, unilateral
+
specific developmental disorders of speech and language (F80.-)
  
*'''[[Q53.111]]''' Unilateral intraabdominal testis
+
stuttering (F80.81)
  
*'''[[Q53.112]]''' Unilateral inguinal testis
+
*'''[[R47.0]]''' Dysphasia and aphasia
  
*'''[[Q53.12]]''' Ectopic perineal testis, unilateral
+
*'''[[R47.01]]''' Aphasia
  
*'''[[Q53.13]]''' Unilateral high scrotal testis
+
''Excludes1''  
  
*'''[[Q53.2]]''' Undescended testicle, bilateral
+
aphasia following cerebrovascular disease (I69. with final characters -20)
  
*'''[[Q53.20]]''' Undescended testicle, unspecified, bilateral
+
progressive isolated aphasia (G31.01)
  
*'''[[Q53.21]]''' Abdominal testis, bilateral
+
*'''[[R47.02]]''' Dysphasia
  
*'''[[Q53.211]]''' Bilateral intraabdominal testes
+
''Excludes1''  
  
*'''[[Q53.212]]''' Bilateral inguinal testes
+
dysphasia following cerebrovascular disease (I69. with final characters -21)
  
*'''[[Q53.22]]''' Ectopic perineal testis, bilateral
+
*'''[[R47.1]]''' Dysarthria and anarthria
  
*'''[[Q53.23]]''' Bilateral high scrotal testes
+
''Excludes1''  
  
*'''[[Q53.9]]''' Undescended testicle, unspecified
+
dysarthria following cerebrovascular disease (I69. with final characters -22)
  
Cryptorchism NOS
+
*'''[[R47.8]]''' Other speech disturbances
  
*'''[[Q54]]''' Hypospadias
+
''Excludes1''  
  
''Excludes1''
+
dysarthria following cerebrovascular disease (I69. with final characters -28)
  
epispadias (Q64.0)
+
*'''[[R47.81]]''' Slurred speech
  
*'''[[Q54.0]]''' Hypospadias, balanic
+
*'''[[R47.82]]''' Fluency disorder in conditions classified elsewhere
  
Hypospadias, coronal
+
Stuttering in conditions classified elsewhere ''Code first''
  
Hypospadias, glandular
+
underlying disease or condition, such as
  
*'''[[Q54.1]]''' Hypospadias, penile
+
Parkinson's disease (G20)
  
*'''[[Q54.2]]''' Hypospadias, penoscrotal
+
''Excludes1''  
  
*'''[[Q54.3]]''' Hypospadias, perineal
+
adult onset fluency disorder (F98.5)
  
*'''[[Q54.4]]''' Congenital chordee
+
childhood onset fluency disorder (F80.81)
  
Chordee without hypospadias
+
fluency disorder (stuttering) following cerebrovascular disease (I69. with final characters -
  
*'''[[Q54.8]]''' Other hypospadias
+
23)
  
Hypospadias with intersex state
+
*'''[[R47.89]]''' Other speech disturbances
  
*'''[[Q54.9]]''' Hypospadias, unspecified
+
*'''[[R47.9]]''' Unspecified speech disturbances
  
*'''[[Q55]]''' Other congenital malformations of male genital organs
+
*'''[[R48]]''' Dyslexia and other symbolic dysfunctions, not elsewhere classified
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital hydrocele (P83.5)  
+
specific developmental disorders of scholastic skills (F81.-)
 +
 
 +
*'''[[R48.0]]''' Dyslexia and alexia
 +
 
 +
*'''[[R48.1]]''' Agnosia
 +
 
 +
Astereognosia (astereognosis)  
  
hypospadias (Q54.-)
+
Autotopagnosia
  
*'''[[Q55.0]]''' Absence and aplasia of testis
+
''Excludes1''  
  
Monorchism
+
visual object agnosia (R48.3)
  
*'''[[Q55.1]]''' Hypoplasia of testis and scrotum
+
*'''[[R48.2]]''' Apraxia
  
Fusion of testes
+
''Excludes1''
  
*'''[[Q55.2]]''' Other and unspecified congenital malformations of testis and scrotum
+
apraxia following cerebrovascular disease (I69. with final characters -90)
  
*'''[[Q55.20]]''' Unspecified congenital malformations of testis and scrotum
+
*'''[[R48.3]]''' Visual agnosia
  
Congenital malformation of testis or scrotum NOS
+
Prosopagnosia
  
*'''[[Q55.21]]''' Polyorchism
+
Simultanagnosia (asimultagnosia)
  
*'''[[Q55.22]]''' Retractile testis
+
*'''[[R48.8]]''' Other symbolic dysfunctions
  
*'''[[Q55.23]]''' Scrotal transposition
+
Acalculia
  
*'''[[Q55.29]]''' Other congenital malformations of testis and scrotum
+
Agraphia
  
*'''[[Q55.3]]''' Atresia of vas deferens ''Code first''
+
*'''[[R48.9]]''' Unspecified symbolic dysfunctions
  
any associated cystic fibrosis (E84.-)
+
*'''[[R49]]''' Voice and resonance disorders
  
*'''[[Q55.4]]''' Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
+
''Excludes1''  
  
Absence or aplasia of prostate
+
psychogenic voice and resonance disorders (F44.4)
  
Absence or aplasia of spermatic cord
+
*'''[[R49.0]]''' Dysphonia
  
Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS
+
Hoarseness
  
*'''[[Q55.5]]''' Congenital absence and aplasia of penis
+
*'''[[R49.1]]''' Aphonia
  
*'''[[Q55.6]]''' Other congenital malformations of penis
+
Loss of voice
  
*'''[[Q55.61]]''' Curvature of penis (lateral)
+
*'''[[R49.2]]''' Hypernasality and hyponasality
  
*'''[[Q55.62]]''' Hypoplasia of penis
+
*'''[[R49.21]]''' Hypernasality
  
Micropenis
+
*'''[[R49.22]]''' Hyponasality
  
*'''[[Q55.63]]''' Congenital torsion of penis
+
*'''[[R49.8]]''' Other voice and resonance disorders
  
''Excludes1''  
+
*'''[[R49.9]]''' Unspecified voice and resonance disorder
  
acquired torsion of penis (N48.82)
+
Change in voice NOS
  
*'''[[Q55.64]]''' Hidden penis
+
'''Resonance disorder NOS '''
  
Buried penis
+
General symptoms and signs (R50-R69)
  
Concealed penis
+
*'''[[R50]]''' Fever of other and unknown origin
  
 
''Excludes1''  
 
''Excludes1''  
  
acquired buried penis (N48.83)
+
chills without fever (R68.83)  
  
*'''[[Q55.69]]''' Other congenital malformation of penis
+
febrile convulsions (R56.0-)
  
Congenital malformation of penis NOS
+
fever of unknown origin during labor (O75.2)
  
*'''[[Q55.7]]''' Congenital vasocutaneous fistula
+
fever of unknown origin in newborn (P81.9)
  
*'''[[Q55.8]]''' Other specified congenital malformations of male genital organs
+
hypothermia due to illness (R68.0)
  
*'''[[Q55.9]]''' Congenital malformation of male genital organ, unspecified
+
malignant hyperthermia due to anesthesia (T88.3)
  
Congenital anomaly of male genital organ
+
puerperal pyrexia NOS (O86.4)
  
Congenital deformity of male genital organ
+
*'''[[R50.2]]''' Drug induced fever ''Use additional''
  
*'''[[Q56]]''' Indeterminate sex and pseudohermaphroditism
+
code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
  
 
''Excludes1''  
 
''Excludes1''  
  
46,XX true hermaphrodite (Q99.1)  
+
postvaccination (postimmunization) fever (R50.83)
 +
 
 +
*'''[[R50.8]]''' Other specified fever
 +
 
 +
*'''[[R50.81]]''' Fever presenting with conditions classified elsewhere ''Code first''
  
androgen insensitivity syndrome (E34.5-)
+
underlying condition when associated fever is present, such as with
  
chimera 46,XX/46,XY true hermaphrodite (Q99.0)  
+
leukemia (C91-C95)  
  
female pseudohermaphroditism with adrenocortical disorder (E25.-)  
+
neutropenia (D70.-)  
  
pseudohermaphroditism with specified chromosomal anomaly (Q96-Q99)  
+
sickle-cell disease (D57.-)
  
pure gonadal dysgenesis (Q99.1)
+
*'''[[R50.82]]''' Postprocedural fever
  
*'''[[Q56.0]]''' Hermaphroditism, not elsewhere classified
+
''Excludes1''  
  
Ovotestis
+
postprocedural infection (T81.4-)
  
*'''[[Q56.1]]''' Male pseudohermaphroditism, not elsewhere classified
+
posttransfusion fever (R50.84)
  
46, XY with streak gonads
+
postvaccination (postimmunization) fever (R50.83)
  
Male pseudohermaphroditism NOS
+
*'''[[R50.83]]''' Postvaccination fever
  
*'''[[Q56.2]]''' Female pseudohermaphroditism, not elsewhere classified
+
Postimmunization fever
  
Female pseudohermaphroditism NOS
+
*'''[[R50.84]]''' Febrile nonhemolytic transfusion reaction
  
*'''[[Q56.3]]''' Pseudohermaphroditism, unspecified
+
FNHTR
  
*'''[[Q56.4]]''' Indeterminate sex, unspecified
+
Posttransfusion fever
  
Ambiguous genitalia
+
*'''[[R50.9]]''' Fever, unspecified
  
Congenital malformations of the urinary system (Q60-Q64)
+
Fever NOS
  
*'''[[Q60]]''' Renal agenesis and other reduction defects of kidney
+
Fever of unknown origin (FUO)
  
''Includes''
+
Fever with chills
  
congenital absence of kidney
+
Fever with rigors
  
congenital atrophy of kidney
+
Hyperpyrexia NOS
  
infantile atrophy of kidney
+
Persistent fever
  
*'''[[Q60.0]]''' Renal agenesis, unilateral
+
Pyrexia NOS
  
*'''[[Q60.1]]''' Renal agenesis, bilateral
+
*'''[[R51]]''' Headache
  
*'''[[Q60.2]]''' Renal agenesis, unspecified
+
Facial pain NOS
  
*'''[[Q60.3]]''' Renal hypoplasia, unilateral
+
''Excludes1''  
  
*'''[[Q60.4]]''' Renal hypoplasia, bilateral
+
atypical face pain (G50.1)
  
*'''[[Q60.5]]''' Renal hypoplasia, unspecified
+
migraine and other headache syndromes (G43-G44)
  
*'''[[Q60.6]]''' Potter's syndrome
+
trigeminal neuralgia (G50.0)
  
*'''[[Q61]]''' Cystic kidney disease
+
*'''[[R52]]''' Pain, unspecified
  
''Excludes1''
+
Acute pain NOS
  
acquired cyst of kidney (N28.1)
+
Generalized pain NOS
  
Potter's syndrome (Q60.6)
+
Pain NOS
  
*'''[[Q61.0]]''' Congenital renal cyst
+
''Excludes1''  
  
*'''[[Q61.00]]''' Congenital renal cyst, unspecified
+
acute and chronic pain, not elsewhere classified (G89.-)
  
Cyst of kidney NOS (congenital)
+
localized pain, unspecified type - code to pain by site, such as
  
*'''[[Q61.01]]''' Congenital single renal cyst
+
abdomen pain (R10.-)
  
*'''[[Q61.02]]''' Congenital multiple renal cysts
+
back pain (M54.9)
  
*'''[[Q61.1]]''' Polycystic kidney, infantile type
+
breast pain (N64.4)
  
Polycystic kidney, autosomal recessive
+
chest pain (R07.1-R07.9)
  
*'''[[Q61.11]]''' Cystic dilatation of collecting ducts
+
ear pain (H92.0-)
  
*'''[[Q61.19]]''' Other polycystic kidney, infantile type
+
eye pain (H57.1)
  
*'''[[Q61.2]]''' Polycystic kidney, adult type
+
headache (R51)
  
Polycystic kidney, autosomal dominant
+
joint pain (M25.5-)
  
*'''[[Q61.3]]''' Polycystic kidney, unspecified
+
limb pain (M79.6-)
  
*'''[[Q61.4]]''' Renal dysplasia
+
lumbar region pain (M54.5)
  
Multicystic dysplastic kidney
+
pelvic and perineal pain (R10.2)
  
Multicystic kidney (development)
+
shoulder pain (M25.51-)  
  
Multicystic kidney disease
+
spine pain (M54.-)
  
Multicystic renal dysplasia
+
throat pain (R07.0)
  
''Excludes1''
+
tongue pain (K14.6)
  
polycystic kidney disease (Q61.11-Q61.3)
+
tooth pain (K08.8)  
  
*'''[[Q61.5]]''' Medullary cystic kidney
+
renal colic (N23)
  
Nephronopthisis
+
pain disorders exclusively related to psychological factors (F45.41)
  
Sponge kidney NOS
+
*'''[[R53]]''' Malaise and fatigue
  
*'''[[Q61.8]]''' Other cystic kidney diseases
+
*'''[[R53.0]]''' Neoplastic (malignant) related fatigue ''Code first''
  
Fibrocystic kidney
+
associated neoplasm
  
Fibrocystic renal degeneration or disease
+
*'''[[R53.1]]''' Weakness
  
*'''[[Q61.9]]''' Cystic kidney disease, unspecified
+
Asthenia NOS
  
Meckel-Gruber syndrome
+
''Excludes1''
  
*'''[[Q62]]''' Congenital obstructive defects of renal pelvis and congenital malformations of ureter
+
age-related weakness (R54)
  
*'''[[Q62.0]]''' Congenital hydronephrosis
+
muscle weakness (M62.8-)
  
*'''[[Q62.1]]''' Congenital occlusion of ureter
+
sarcopenia (M62.84)
  
Atresia and stenosis of ureter
+
senile asthenia (R54)
  
*'''[[Q62.10]]''' Congenital occlusion of ureter, unspecified
+
*'''[[R53.2]]''' Functional quadriplegia
  
*'''[[Q62.11]]''' Congenital occlusion of ureteropelvic junction
+
Complete immobility due to severe physical disability or frailty
  
*'''[[Q62.12]]''' Congenital occlusion of ureterovesical orifice
+
''Excludes1''  
  
*'''[[Q62.2]]''' Congenital megaureter
+
frailty NOS (R54)
  
Congenital dilatation of ureter
+
hysterical paralysis (F44.4)
  
*'''[[Q62.3]]''' Other obstructive defects of renal pelvis and ureter
+
immobility syndrome (M62.3)
  
*'''[[Q62.31]]''' Congenital ureterocele, orthotopic
+
neurologic quadriplegia (G82.5-)
  
*'''[[Q62.32]]''' Cecoureterocele
+
quadriplegia (G82.50)
  
Ectopic ureterocele
+
*'''[[R53.8]]''' Other malaise and fatigue
  
*'''[[Q62.39]]''' Other obstructive defects of renal pelvis and ureter
+
''Excludes1''  
  
Ureteropelvic junction obstruction NOS
+
combat exhaustion and fatigue (F43.0)
  
*'''[[Q62.4]]''' Agenesis of ureter
+
congenital debility (P96.9)
  
Congenital absence ureter
+
exhaustion and fatigue due to excessive exertion (T73.3)
  
*'''[[Q62.5]]''' Duplication of ureter
+
exhaustion and fatigue due to exposure (T73.2)
  
Accessory ureter
+
exhaustion and fatigue due to heat (T67.-)
  
Double ureter
+
exhaustion and fatigue due to pregnancy (O26.8-)
  
*'''[[Q62.6]]''' Malposition of ureter
+
exhaustion and fatigue due to recurrent depressive episode (F33)
  
*'''[[Q62.60]]''' Malposition of ureter, unspecified
+
exhaustion and fatigue due to senile debility (R54)
  
*'''[[Q62.61]]''' Deviation of ureter
+
*'''[[R53.81]]''' Other malaise
  
*'''[[Q62.62]]''' Displacement of ureter
+
Chronic debility
  
*'''[[Q62.63]]''' Anomalous implantation of ureter
+
Debility NOS
  
Ectopia of ureter
+
General physical deterioration
  
Ectopic ureter
+
Malaise NOS
  
*'''[[Q62.69]]''' Other malposition of ureter
+
Nervous debility
  
*'''[[Q62.7]]''' Congenital vesico-uretero-renal reflux
+
''Excludes1''  
  
*'''[[Q62.8]]''' Other congenital malformations of ureter
+
age-related physical debility (R54)
  
Anomaly of ureter NOS
+
*'''[[R53.82]]''' Chronic fatigue, unspecified
  
*'''[[Q63]]''' Other congenital malformations of kidney
+
Chronic fatigue syndrome NOS
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital nephrotic syndrome (N04.-)
+
postviral fatigue syndrome (G93.3)
 +
 
 +
*'''[[R53.83]]''' Other fatigue
  
*'''[[Q63.0]]''' Accessory kidney
+
Fatigue NOS
  
*'''[[Q63.1]]''' Lobulated, fused and horseshoe kidney
+
Lack of energy
  
*'''[[Q63.2]]''' Ectopic kidney
+
Lethargy
  
Congenital displaced kidney
+
Tiredness
  
Malrotation of kidney
+
''Excludes2''
  
*'''[[Q63.3]]''' Hyperplastic and giant kidney
+
exhaustion and fatigue due to depressive episode (F32.-)
  
Compensatory hypertrophy of kidney
+
*'''[[R54]]''' Age-related physical debility
  
*'''[[Q63.8]]''' Other specified congenital malformations of kidney
+
Frailty
  
Congenital renal calculi
+
Old age
  
*'''[[Q63.9]]''' Congenital malformation of kidney, unspecified
+
Senescence
  
*'''[[Q64]]''' Other congenital malformations of urinary system
+
Senile asthenia
  
*'''[[Q64.0]]''' Epispadias
+
Senile debility
  
 
''Excludes1''  
 
''Excludes1''  
  
hypospadias (Q54.-)
+
age-related cognitive decline (R41.81)  
  
*'''[[Q64.1]]''' Exstrophy of urinary bladder
+
sarcopenia (M62.84)
  
*'''[[Q64.10]]''' Exstrophy of urinary bladder, unspecified
+
senile psychosis (F03)
  
Ectopia vesicae
+
senility NOS (R41.81)
  
*'''[[Q64.11]]''' Supravesical fissure of urinary bladder
+
*'''[[R55]]''' Syncope and collapse
  
*'''[[Q64.12]]''' Cloacal exstrophy of urinary bladder
+
Blackout
  
*'''[[Q64.19]]''' Other exstrophy of urinary bladder
+
Fainting
  
Extroversion of bladder
+
Vasovagal attack
  
*'''[[Q64.2]]''' Congenital posterior urethral valves
+
''Excludes1''  
  
*'''[[Q64.3]]''' Other atresia and stenosis of urethra and bladder neck
+
cardiogenic shock (R57.0)
  
*'''[[Q64.31]]''' Congenital bladder neck obstruction
+
carotid sinus syncope (G90.01)
  
Congenital obstruction of vesicourethral orifice
+
heat syncope (T67.1)
  
*'''[[Q64.32]]''' Congenital stricture of urethra
+
neurocirculatory asthenia (F45.8)
  
*'''[[Q64.33]]''' Congenital stricture of urinary meatus
+
neurogenic orthostatic hypotension (G90.3)
  
*'''[[Q64.39]]''' Other atresia and stenosis of urethra and bladder neck
+
orthostatic hypotension (I95.1)
  
Atresia and stenosis of urethra and bladder neck NOS
+
postprocedural shock (T81.1-)
  
*'''[[Q64.4]]''' Malformation of urachus
+
psychogenic syncope (F48.8)
  
Cyst of urachus
+
shock NOS (R57.9)
  
Patent urachus
+
shock complicating or following abortion or ectopic or molar pregnancy (O00-O07, O08.3)
  
Prolapse of urachus
+
shock complicating or following labor and delivery (O75.1)
  
*'''[[Q64.5]]''' Congenital absence of bladder and urethra
+
Stokes-Adams attack (I45.9)
  
*'''[[Q64.6]]''' Congenital diverticulum of bladder
+
unconsciousness NOS (R40.2-)
  
*'''[[Q64.7]]''' Other and unspecified congenital malformations of bladder and urethra
+
*'''[[R56]]''' Convulsions, not elsewhere classified
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital prolapse of bladder (mucosa) (Q79.4)
+
dissociative convulsions and seizures (F44.5)  
  
*'''[[Q64.70]]''' Unspecified congenital malformation of bladder and urethra
+
epileptic convulsions and seizures (G40.-)
  
Malformation of bladder or urethra NOS
+
newborn convulsions and seizures (P90)
  
*'''[[Q64.71]]''' Congenital prolapse of urethra
+
*'''[[R56.0]]''' Febrile convulsions
  
*'''[[Q64.72]]''' Congenital prolapse of urinary meatus
+
*'''[[R56.00]]''' Simple febrile convulsions
  
*'''[[Q64.73]]''' Congenital urethrorectal fistula
+
Febrile convulsion NOS
  
*'''[[Q64.74]]''' Double urethra
+
Febrile seizure NOS
  
*'''[[Q64.75]]''' Double urinary meatus
+
*'''[[R56.01]]''' Complex febrile convulsions
  
*'''[[Q64.79]]''' Other congenital malformations of bladder and urethra
+
Atypical febrile seizure
  
*'''[[Q64.8]]''' Other specified congenital malformations of urinary system
+
Complex febrile seizure
  
*'''[[Q64.9]]''' Congenital malformation of urinary system, unspecified
+
Complicated febrile seizure
  
Congenital anomaly NOS of urinary system
+
''Excludes1''
  
Congenital deformity NOS of urinary system
+
status epilepticus (G40.901)
  
Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
+
*'''[[R56.1]]''' Post traumatic seizures
 
 
*'''[[Q65]]''' Congenital deformities of hip
 
  
 
''Excludes1''  
 
''Excludes1''  
  
clicking hip (R29.4)
+
post traumatic epilepsy (G40.-)
  
*'''[[Q65.0]]''' Congenital dislocation of hip, unilateral
+
*'''[[R56.9]]''' Unspecified convulsions
  
*'''[[Q65.00]]''' Congenital dislocation of unspecified hip, unilateral
+
Convulsion disorder
  
*'''[[Q65.01]]''' Congenital dislocation of right hip, unilateral
+
Fit NOS
  
*'''[[Q65.02]]''' Congenital dislocation of left hip, unilateral
+
'''Recurrent convulsions'''
  
*'''[[Q65.1]]''' Congenital dislocation of hip, bilateral
+
Seizure(s) (convulsive) NOS
  
*'''[[Q65.2]]''' Congenital dislocation of hip, unspecified
+
*'''[[R57]]''' Shock, not elsewhere classified
  
*'''[[Q65.3]]''' Congenital partial dislocation of hip, unilateral
+
''Excludes1''  
  
*'''[[Q65.30]]''' Congenital partial dislocation of unspecified hip, unilateral
+
anaphylactic shock NOS (T78.2)
  
*'''[[Q65.31]]''' Congenital partial dislocation of right hip, unilateral
+
anaphylactic reaction or shock due to adverse food reaction (T78.0-)
  
*'''[[Q65.32]]''' Congenital partial dislocation of left hip, unilateral
+
anaphylactic shock due to adverse effect of correct drug or medicament properly administered (T88.6)
  
*'''[[Q65.4]]''' Congenital partial dislocation of hip, bilateral
+
anaphylactic shock due to serum (T80.5-)
  
*'''[[Q65.5]]''' Congenital partial dislocation of hip, unspecified
+
anesthetic shock (T88.3)
  
*'''[[Q65.6]]''' Congenital unstable hip
+
electric shock (T75.4)
  
Congenital dislocatable hip
+
obstetric shock (O75.1)
  
*'''[[Q65.8]]''' Other congenital deformities of hip
+
postprocedural shock (T81.1-)
  
*'''[[Q65.81]]''' Congenital coxa valga
+
psychic shock (F43.0)
  
*'''[[Q65.82]]''' Congenital coxa vara
+
shock complicating or following ectopic or molar pregnancy (O00-O07, O08.3)
  
*'''[[Q65.89]]''' Other specified congenital deformities of hip
+
shock due to lightning (T75.01)
  
Anteversion of femoral neck
+
traumatic shock (T79.4)
  
Congenital acetabular dysplasia
+
toxic shock syndrome (A48.3)
  
*'''[[Q65.9]]''' Congenital deformity of hip, unspecified
+
*'''[[R57.0]]''' Cardiogenic shock
  
*'''[[Q66]]''' Congenital deformities of feet
+
''Excludes2''  
  
''Excludes1''
+
septic shock (R65.21)
  
reduction defects of feet (Q72.-)
+
*'''[[R57.1]]''' Hypovolemic shock
  
valgus deformities (acquired) (M21.0-)
+
*'''[[R57.8]]''' Other shock
  
varus deformities (acquired) (M21.1-)
+
*'''[[R57.9]]''' Shock, unspecified
  
*'''[[Q66.0]]''' Congenital talipes equinovarus
+
Failure of peripheral circulation NOS
  
*'''[[Q66.00]]''' Congenital talipes equinovarus, unspecified foot
+
*'''[[R58]]''' Hemorrhage, not elsewhere classified
  
*'''[[Q66.01]]''' Congenital talipes equinovarus, right foot
+
Hemorrhage NOS
  
*'''[[Q66.02]]''' Congenital talipes equinovarus, left foot
+
''Excludes1''  
  
*'''[[Q66.1]]''' Congenital talipes calcaneovarus
+
hemorrhage included with underlying conditions, such as
  
*'''[[Q66.10]]''' Congenital talipes calcaneovarus, unspecified foot
+
acute duodenal ulcer with hemorrhage (K26.0)
  
*'''[[Q66.11]]''' Congenital talipes calcaneovarus, right foot
+
acute gastritis with bleeding (K29.01)
  
*'''[[Q66.12]]''' Congenital talipes calcaneovarus, left foot
+
ulcerative enterocolitis with rectal bleeding (K51.01)
  
*'''[[Q66.2]]''' Congenital metatarsus (primus) varus
+
*'''[[R59]]''' Enlarged lymph nodes
  
*'''[[Q66.21]]''' Congenital metatarsus primus varus
+
''Includes''  
  
*'''[[Q66.211]]''' Congenital metatarsus primus varus, right foot
+
swollen glands
  
*'''[[Q66.212]]''' Congenital metatarsus primus varus, left foot
+
''Excludes1''  
  
*'''[[Q66.219]]''' Congenital metatarsus primus varus, unspecified foot
+
lymphadenitis NOS (I88.9)
  
*'''[[Q66.22]]''' Congenital metatarsus adductus
+
acute lymphadenitis (L04.-)
  
Congenital metatarsus varus
+
chronic lymphadenitis (I88.1)
  
*'''[[Q66.221]]''' Congenital metatarsus adductus, right foot
+
mesenteric (acute) (chronic) lymphadenitis (I88.0)
  
*'''[[Q66.222]]''' Congenital metatarsus adductus, left foot
+
*'''[[R59.0]]''' Localized enlarged lymph nodes
  
*'''[[Q66.229]]''' Congenital metatarsus adductus, unspecified foot
+
*'''[[R59.1]]''' Generalized enlarged lymph nodes
  
*'''[[Q66.3]]''' Other congenital varus deformities of feet
+
Lymphadenopathy NOS
  
Hallux varus, congenital
+
*'''[[R59.9]]''' Enlarged lymph nodes, unspecified
  
*'''[[Q66.30]]''' Other congenital varus deformities of feet, unspecified foot
+
*'''[[R60]]''' Edema, not elsewhere classified
  
*'''[[Q66.31]]''' Other congenital varus deformities of feet, right foot
+
''Excludes1''  
  
*'''[[Q66.32]]''' Other congenital varus deformities of feet, left foot
+
angioneurotic edema (T78.3)
  
*'''[[Q66.4]]''' Congenital talipes calcaneovalgus
+
ascites (R18.-)
  
*'''[[Q66.40]]''' Congenital talipes calcaneovalgus, unspecified foot
+
cerebral edema (G93.6)
  
*'''[[Q66.41]]''' Congenital talipes calcaneovalgus, right foot
+
cerebral edema due to birth injury (P11.0)
  
*'''[[Q66.42]]''' Congenital talipes calcaneovalgus, left foot
+
edema of larynx (J38.4)
  
*'''[[Q66.5]]''' Congenital pes planus
+
edema of nasopharynx (J39.2)
  
Congenital flat foot
+
edema of pharynx (J39.2)
  
Congenital rigid flat foot
+
gestational edema (O12.0-)
  
Congenital spastic (everted) flat foot
+
hereditary edema (Q82.0)  
  
''Excludes1''
+
hydrops fetalis NOS (P83.2)
  
pes planus, acquired (M21.4)
+
hydrothorax (J94.8)  
  
*'''[[Q66.50]]''' Congenital pes planus, unspecified foot
+
hydrops fetalis NOS (P83.2)
  
*'''[[Q66.51]]''' Congenital pes planus, right foot
+
newborn edema (P83.3)
  
*'''[[Q66.52]]''' Congenital pes planus, left foot
+
pulmonary edema (J81.-)
  
*'''[[Q66.6]]''' Other congenital valgus deformities of feet
+
*'''[[R60.0]]''' Localized edema
  
Congenital metatarsus valgus
+
*'''[[R60.1]]''' Generalized edema
  
*'''[[Q66.7]]''' Congenital pes cavus
+
''Excludes2''  
  
*'''[[Q66.70]]''' Congenital pes cavus, unspecified foot
+
nutritional edema (E40-E46)
  
*'''[[Q66.71]]''' Congenital pes cavus, right foot
+
*'''[[R60.9]]''' Edema, unspecified
  
*'''[[Q66.72]]''' Congenital pes cavus, left foot
+
Fluid retention NOS
  
*'''[[Q66.8]]''' Other congenital deformities of feet
+
*'''[[R61]]''' Generalized hyperhidrosis
  
*'''[[Q66.80]]''' Congenital vertical talus deformity, unspecified foot
+
Excessive sweating
  
*'''[[Q66.81]]''' Congenital vertical talus deformity, right foot
+
Night sweats
  
*'''[[Q66.82]]''' Congenital vertical talus deformity, left foot
+
Secondary hyperhidrosis ''Code first''  
  
*'''[[Q66.89]]''' Other specified congenital deformities of feet
+
, if applicable, menopausal and female climacteric states (N95.1)
  
Congenital asymmetric talipes
+
''Excludes1''
  
Congenital clubfoot NOS
+
focal (primary) (secondary) hyperhidrosis (L74.5-)
  
Congenital talipes NOS
+
Frey's syndrome (L74.52)
  
Congenital tarsal coalition
+
localized (primary) (secondary) hyperhidrosis (L74.5-)
  
Hammer toe, congenital
+
*'''[[R62]]''' Lack of expected normal physiological development in childhood and adults
  
*'''[[Q66.9]]''' Congenital deformity of feet, unspecified
+
''Excludes1''  
  
*'''[[Q66.90]]''' Congenital deformity of feet, unspecified, unspecified foot
+
delayed puberty (E30.0)
  
*'''[[Q66.91]]''' Congenital deformity of feet, unspecified, right foot
+
gonadal dysgenesis (Q99.1)
  
*'''[[Q66.92]]''' Congenital deformity of feet, unspecified, left foot
+
hypopituitarism (E23.0)
  
*'''[[Q67]]''' Congenital musculoskeletal deformities of head, face, spine and chest
+
*'''[[R62.0]]''' Delayed milestone in childhood
  
''Excludes1''
+
Delayed attainment of expected physiological developmental stage
  
congenital malformation syndromes classified to Q87.-
+
Late talker
  
Potter's syndrome (Q60.6)
+
Late walker
  
*'''[[Q67.0]]''' Congenital facial asymmetry
+
*'''[[R62.5]]''' Other and unspecified lack of expected normal physiological development in childhood
  
*'''[[Q67.1]]''' Congenital compression facies
+
''Excludes1''  
 
 
*'''[[Q67.2]]''' Dolichocephaly
 
  
*'''[[Q67.3]]''' Plagiocephaly
+
HIV disease resulting in failure to thrive (B20)
  
*'''[[Q67.4]]''' Other congenital deformities of skull, face and jaw
+
physical retardation due to malnutrition (E45)
  
Congenital depressions in skull
+
*'''[[R62.50]]''' Unspecified lack of expected normal physiological development in childhood
  
Congenital hemifacial atrophy or hypertrophy
+
Infantilism NOS
  
Deviation of nasal septum, congenital
+
*'''[[R62.51]]''' Failure to thrive (child)
  
Squashed or bent nose, congenital
+
Failure to gain weight
  
 
''Excludes1''  
 
''Excludes1''  
  
dentofacial anomalies (including malocclusion) (M26.-)  
+
failure to thrive in child under 28 days old (P92.6)
  
syphilitic saddle nose (A50.5)
+
*'''[[R62.52]]''' Short stature (child)
  
*'''[[Q67.5]]''' Congenital deformity of spine
+
Lack of growth
  
Congenital postural scoliosis
+
Physical retardation
  
Congenital scoliosis NOS  
+
Short stature NOS  
  
 
''Excludes1''  
 
''Excludes1''  
  
infantile idiopathic scoliosis (M41.0)  
+
short stature due to endocrine disorder (E34.3)
  
scoliosis due to congenital bony malformation (Q76.3)
+
*'''[[R62.59]]''' Other lack of expected normal physiological development in childhood
  
*'''[[Q67.6]]''' Pectus excavatum
+
*'''[[R62.7]]''' Adult failure to thrive
  
Congenital funnel chest
+
*'''[[R63]]''' Symptoms and signs concerning food and fluid intake
  
*'''[[Q67.7]]''' Pectus carinatum
+
''Excludes1''  
 
 
Congenital pigeon chest
 
  
*'''[[Q67.8]]''' Other congenital deformities of chest
+
bulimia NOS (F50.2)
  
Congenital deformity of chest wall NOS
+
*'''[[R63.0]]''' Anorexia
  
*'''[[Q68]]''' Other congenital musculoskeletal deformities
+
Loss of appetite
  
 
''Excludes1''  
 
''Excludes1''  
  
reduction defects of limb(s) (Q71-Q73)  
+
anorexia nervosa (F50.0-)  
  
''Excludes2''
+
loss of appetite of nonorganic origin (F50.89)
  
congenital myotonic chondrodystrophy (G71.13)
+
*'''[[R63.1]]''' Polydipsia
  
*'''[[Q68.0]]''' Congenital deformity of sternocleidomastoid muscle
+
Excessive thirst
  
Congenital contracture of sternocleidomastoid (muscle)
+
*'''[[R63.2]]''' Polyphagia
  
Congenital (sternomastoid) torticollis
+
Excessive eating
  
Sternomastoid tumor (congenital)
+
Hyperalimentation NOS
  
*'''[[Q68.1]]''' Congenital deformity of finger(s) and hand
+
*'''[[R63.3]]''' Feeding difficulties
  
Congenital clubfinger
+
Feeding problem (elderly) (infant) NOS
  
Spade-like hand (congenital)
+
Picky eater
  
*'''[[Q68.2]]''' Congenital deformity of knee
+
''Excludes1''  
  
Congenital dislocation of knee
+
eating disorders (F50.-)
  
Congenital genu recurvatum
+
feeding problems of newborn (P92.-)
  
*'''[[Q68.3]]''' Congenital bowing of femur
+
infant feeding disorder of nonorganic origin (F98.2-)
  
''Excludes1''  
+
*'''[[R63.4]]''' Abnormal weight loss
  
anteversion of femur (neck) (Q65.89)
+
*'''[[R63.5]]''' Abnormal weight gain
  
*'''[[Q68.4]]''' Congenital bowing of tibia and fibula
+
''Excludes1''  
  
*'''[[Q68.5]]''' Congenital bowing of long bones of leg, unspecified
+
excessive weight gain in pregnancy (O26.0-)
  
*'''[[Q68.6]]''' Discoid meniscus
+
obesity (E66.-)
  
*'''[[Q68.8]]''' Other specified congenital musculoskeletal deformities
+
*'''[[R63.6]]''' Underweight ''Use additional''
  
Congenital deformity of clavicle
+
code to identify body mass index (BMI), if known (Z68.-)
  
Congenital deformity of elbow
+
''Excludes1''
  
Congenital deformity of forearm
+
abnormal weight loss (R63.4)
  
Congenital deformity of scapula
+
anorexia nervosa (F50.0-)
  
Congenital deformity of wrist
+
malnutrition (E40-E46)
  
Congenital dislocation of elbow
+
*'''[[R63.8]]''' Other symptoms and signs concerning food and fluid intake
  
Congenital dislocation of shoulder
+
*'''[[R64]]''' Cachexia
  
Congenital dislocation of wrist
+
Wasting syndrome ''Code first''
  
*'''[[Q69]]''' Polydactyly
+
underlying condition, if known
  
*'''[[Q69.0]]''' Accessory finger(s)
+
''Excludes1''  
  
*'''[[Q69.1]]''' Accessory thumb(s)
+
abnormal weight loss (R63.4)  
  
*'''[[Q69.2]]''' Accessory toe(s)
+
nutritional marasmus (E41)
  
Accessory hallux
+
*'''[[R65]]''' Symptoms and signs specifically associated with systemic inflammation and infection
  
*'''[[Q69.9]]''' Polydactyly, unspecified
+
*'''[[R65.1]]''' Systemic inflammatory response syndrome (SIRS) of non-infectious origin ''Code first''
  
Supernumerary digit(s) NOS
+
underlying condition, such as
  
*'''[[Q70]]''' Syndactyly
+
heatstroke (T67.0-)
  
*'''[[Q70.0]]''' Fused fingers
+
injury and trauma (S00-T88)
  
Complex syndactyly of fingers with synostosis
+
''Excludes1''
  
*'''[[Q70.00]]''' Fused fingers, unspecified hand
+
sepsis- code to infection
  
*'''[[Q70.01]]''' Fused fingers, right hand
+
severe sepsis (R65.2)
  
*'''[[Q70.02]]''' Fused fingers, left hand
+
*'''[[R65.10]]''' Systemic inflammatory response syndrome (SIRS) of non-infectious origin without acute organ
  
*'''[[Q70.03]]''' Fused fingers, bilateral
+
dysfunction
  
*'''[[Q70.1]]''' Webbed fingers
+
Systemic inflammatory response syndrome (SIRS) NOS
  
Simple syndactyly of fingers without synostosis
+
*'''[[R65.11]]''' Systemic inflammatory response syndrome (SIRS) of non-infectious origin with acute organ
  
*'''[[Q70.10]]''' Webbed fingers, unspecified hand
+
dysfunction ''Use additional''  
  
*'''[[Q70.11]]''' Webbed fingers, right hand
+
code to identify specific acute organ dysfunction, such as
  
*'''[[Q70.12]]''' Webbed fingers, left hand
+
acute kidney failure (N17.-)
  
*'''[[Q70.13]]''' Webbed fingers, bilateral
+
acute respiratory failure (J96.0-)
  
*'''[[Q70.2]]''' Fused toes
+
critical illness myopathy (G72.81)
  
Complex syndactyly of toes with synostosis
+
critical illness polyneuropathy (G62.81)
  
*'''[[Q70.20]]''' Fused toes, unspecified foot
+
disseminated intravascular coagulopathy (DIC) (D65)
  
*'''[[Q70.21]]''' Fused toes, right foot
+
encephalopathy (metabolic) (septic) (G93.41)
  
*'''[[Q70.22]]''' Fused toes, left foot
+
hepatic failure (K72.0-)
  
*'''[[Q70.23]]''' Fused toes, bilateral
+
*'''[[R65.2]]''' Severe sepsis
  
*'''[[Q70.3]]''' Webbed toes
+
Infection with associated acute organ dysfunction
  
Simple syndactyly of toes without synostosis
+
Sepsis with acute organ dysfunction
  
*'''[[Q70.30]]''' Webbed toes, unspecified foot
+
Sepsis with multiple organ dysfunction
  
*'''[[Q70.31]]''' Webbed toes, right foot
+
Systemic inflammatory response syndrome due to infectious process with acute organ dysfunction ''Code first''  
  
*'''[[Q70.32]]''' Webbed toes, left foot
+
underlying infection, such as
  
*'''[[Q70.33]]''' Webbed toes, bilateral
+
infection following a procedure (T81.4-)
  
*'''[[Q70.4]]''' Polysyndactyly, unspecified
+
infections following infusion, transfusion and therapeutic injection (T80.2-)
  
''Excludes1''
+
puerperal sepsis (O85)
  
specified syndactyly of hand and feet - code to specified conditions (Q70.0- -Q70.3-)
+
sepsis following complete or unspecified spontaneous abortion (O03.87)  
  
*'''[[Q70.9]]''' Syndactyly, unspecified
+
sepsis following ectopic and molar pregnancy (O08.82)
  
Symphalangy NOS
+
sepsis following incomplete spontaneous abortion (O03.37)
  
*'''[[Q71]]''' Reduction defects of upper limb
+
sepsis following (induced) termination of pregnancy (O04.87)
  
*'''[[Q71.0]]''' Congenital complete absence of upper limb
+
sepsis NOS (A41.9) ''Use additional''  
  
*'''[[Q71.00]]''' Congenital complete absence of unspecified upper limb
+
code to identify specific acute organ dysfunction, such as
  
*'''[[Q71.01]]''' Congenital complete absence of right upper limb
+
acute kidney failure (N17.-)
  
*'''[[Q71.02]]''' Congenital complete absence of left upper limb
+
acute respiratory failure (J96.0-)
  
*'''[[Q71.03]]''' Congenital complete absence of upper limb, bilateral
+
critical illness myopathy (G72.81)
  
*'''[[Q71.1]]''' Congenital absence of upper arm and forearm with hand present
+
critical illness polyneuropathy (G62.81)
  
*'''[[Q71.10]]''' Congenital absence of unspecified upper arm and forearm with hand present
+
disseminated intravascular coagulopathy (DIC) (D65)
  
*'''[[Q71.11]]''' Congenital absence of right upper arm and forearm with hand present
+
encephalopathy (metabolic) (septic) (G93.41)
  
*'''[[Q71.12]]''' Congenital absence of left upper arm and forearm with hand present
+
hepatic failure (K72.0-)
  
*'''[[Q71.13]]''' Congenital absence of upper arm and forearm with hand present, bilateral
+
*'''[[R65.20]]''' Severe sepsis without septic shock
  
*'''[[Q71.2]]''' Congenital absence of both forearm and hand
+
Severe sepsis NOS
  
*'''[[Q71.20]]''' Congenital absence of both forearm and hand, unspecified upper limb
+
*'''[[R65.21]]''' Severe sepsis with septic shock
  
*'''[[Q71.21]]''' Congenital absence of both forearm and hand, right upper limb
+
*'''[[R68]]''' Other general symptoms and signs
  
*'''[[Q71.22]]''' Congenital absence of both forearm and hand, left upper limb
+
*'''[[R68.0]]''' Hypothermia, not associated with low environmental temperature
  
*'''[[Q71.23]]''' Congenital absence of both forearm and hand, bilateral
+
''Excludes1''  
  
*'''[[Q71.3]]''' Congenital absence of hand and finger
+
hypothermia NOS (accidental) (T68)
  
*'''[[Q71.30]]''' Congenital absence of unspecified hand and finger
+
hypothermia due to anesthesia (T88.51)
  
*'''[[Q71.31]]''' Congenital absence of right hand and finger
+
hypothermia due to low environmental temperature (T68)
  
*'''[[Q71.32]]''' Congenital absence of left hand and finger
+
newborn hypothermia (P80.-)
  
*'''[[Q71.33]]''' Congenital absence of hand and finger, bilateral
+
*'''[[R68.1]]''' Nonspecific symptoms peculiar to infancy
  
*'''[[Q71.4]]''' Longitudinal reduction defect of radius
+
''Excludes1''  
  
Clubhand (congenital)
+
colic, infantile (R10.83)  
  
Radial clubhand
+
neonatal cerebral irritability (P91.3)
  
*'''[[Q71.40]]''' Longitudinal reduction defect of unspecified radius
+
teething syndrome (K00.7)
  
*'''[[Q71.41]]''' Longitudinal reduction defect of right radius
+
*'''[[R68.11]]''' Excessive crying of infant (baby)
  
*'''[[Q71.42]]''' Longitudinal reduction defect of left radius
+
''Excludes1''  
  
*'''[[Q71.43]]''' Longitudinal reduction defect of radius, bilateral
+
excessive crying of child, adolescent, or adult (R45.83)
  
*'''[[Q71.5]]''' Longitudinal reduction defect of ulna
+
*'''[[R68.12]]''' Fussy infant (baby)
  
*'''[[Q71.50]]''' Longitudinal reduction defect of unspecified ulna
+
Irritable infant
  
*'''[[Q71.51]]''' Longitudinal reduction defect of right ulna
+
*'''[[R68.13]]''' Apparent life threatening event in infant (ALTE)
  
*'''[[Q71.52]]''' Longitudinal reduction defect of left ulna
+
Apparent life threatening event in newborn
  
*'''[[Q71.53]]''' Longitudinal reduction defect of ulna, bilateral
+
Brief resolved unexplained event (BRUE) ''Code first''  
  
*'''[[Q71.6]]''' Lobster-claw hand
+
confirmed diagnosis, if known ''Use additional''  
  
*'''[[Q71.60]]''' Lobster-claw hand, unspecified hand
+
code(s) for associated signs and symptoms if no confirmed diagnosis established, or if
  
*'''[[Q71.61]]''' Lobster-claw right hand
+
signs and symptoms are not associated routinely with confirmed diagnosis, or
  
*'''[[Q71.62]]''' Lobster-claw left hand
+
provide additional information for cause of ALTE
  
*'''[[Q71.63]]''' Lobster-claw hand, bilateral
+
*'''[[R68.19]]''' Other nonspecific symptoms peculiar to infancy
  
*'''[[Q71.8]]''' Other reduction defects of upper limb
+
*'''[[R68.2]]''' Dry mouth, unspecified
  
*'''[[Q71.81]]''' Congenital shortening of upper limb
+
''Excludes1''  
  
*'''[[Q71.811]]''' Congenital shortening of right upper limb
+
dry mouth due to dehydration (E86.0)
  
*'''[[Q71.812]]''' Congenital shortening of left upper limb
+
dry mouth due to sicca syndrome (Sjögren) (M35.0-)
  
*'''[[Q71.813]]''' Congenital shortening of upper limb, bilateral
+
salivary gland hyposecretion (K11.7)
  
*'''[[Q71.819]]''' Congenital shortening of unspecified upper limb
+
*'''[[R68.3]]''' Clubbing of fingers
  
*'''[[Q71.89]]''' Other reduction defects of upper limb
+
Clubbing of nails
  
*'''[[Q71.891]]''' Other reduction defects of right upper limb
+
''Excludes1''  
  
*'''[[Q71.892]]''' Other reduction defects of left upper limb
+
congenital clubfinger (Q68.1)
  
*'''[[Q71.893]]''' Other reduction defects of upper limb, bilateral
+
*'''[[R68.8]]''' Other general symptoms and signs
  
*'''[[Q71.899]]''' Other reduction defects of unspecified upper limb
+
*'''[[R68.81]]''' Early satiety
  
*'''[[Q71.9]]''' Unspecified reduction defect of upper limb
+
*'''[[R68.82]]''' Decreased libido
  
*'''[[Q71.90]]''' Unspecified reduction defect of unspecified upper limb
+
Decreased sexual desire
  
*'''[[Q71.91]]''' Unspecified reduction defect of right upper limb
+
*'''[[R68.83]]''' Chills (without fever)
  
*'''[[Q71.92]]''' Unspecified reduction defect of left upper limb
+
Chills NOS
  
*'''[[Q71.93]]''' Unspecified reduction defect of upper limb, bilateral
+
''Excludes1''  
  
*'''[[Q72]]''' Reduction defects of lower limb
+
chills with fever (R50.9)
  
*'''[[Q72.0]]''' Congenital complete absence of lower limb
+
*'''[[R68.84]]''' Jaw pain
  
*'''[[Q72.00]]''' Congenital complete absence of unspecified lower limb
+
Mandibular pain
  
*'''[[Q72.01]]''' Congenital complete absence of right lower limb
+
Maxilla pain
  
*'''[[Q72.02]]''' Congenital complete absence of left lower limb
+
''Excludes1''  
  
*'''[[Q72.03]]''' Congenital complete absence of lower limb, bilateral
+
temporomandibular joint arthralgia (M26.62-)
  
*'''[[Q72.1]]''' Congenital absence of thigh and lower leg with foot present
+
*'''[[R68.89]]''' Other general symptoms and signs
  
*'''[[Q72.10]]''' Congenital absence of unspecified thigh and lower leg with foot present
+
*'''[[R69]]''' Illness, unspecified
  
*'''[[Q72.11]]''' Congenital absence of right thigh and lower leg with foot present
+
Unknown and unspecified cases of morbidity
  
*'''[[Q72.12]]''' Congenital absence of left thigh and lower leg with foot present
+
Abnormal findings on examination of blood, without diagnosis (R70-R79)
  
*'''[[Q72.13]]''' Congenital absence of thigh and lower leg with foot present, bilateral
+
''Excludes2''  
  
*'''[[Q72.2]]''' Congenital absence of both lower leg and foot
+
abnormal findings on antenatal screening of mother (O28.-)
  
*'''[[Q72.20]]''' Congenital absence of both lower leg and foot, unspecified lower limb
+
abnormalities of lipids (E78.-)
  
*'''[[Q72.21]]''' Congenital absence of both lower leg and foot, right lower limb
+
abnormalities of platelets and thrombocytes (D69.-)
  
*'''[[Q72.22]]''' Congenital absence of both lower leg and foot, left lower limb
+
abnormalities of white blood cells classified elsewhere (D70-D72)
  
*'''[[Q72.23]]''' Congenital absence of both lower leg and foot, bilateral
+
coagulation hemorrhagic disorders (D65-D68)
  
*'''[[Q72.3]]''' Congenital absence of foot and toe(s)
+
diagnostic abnormal findings classified elsewhere - see Alphabetical Index
  
*'''[[Q72.30]]''' Congenital absence of unspecified foot and toe(s)
+
hemorrhagic and hematological disorders of newborn (P50-P61)
  
*'''[[Q72.31]]''' Congenital absence of right foot and toe(s)
+
*'''[[R70]]''' Elevated erythrocyte sedimentation rate and abnormality of plasma viscosity
  
*'''[[Q72.32]]''' Congenital absence of left foot and toe(s)
+
*'''[[R70.0]]''' Elevated erythrocyte sedimentation rate
  
*'''[[Q72.33]]''' Congenital absence of foot and toe(s), bilateral
+
*'''[[R70.1]]''' Abnormal plasma viscosity
  
*'''[[Q72.4]]''' Longitudinal reduction defect of femur
+
*'''[[R71]]''' Abnormality of red blood cells
  
Proximal femoral focal deficiency
+
''Excludes1''
  
*'''[[Q72.40]]''' Longitudinal reduction defect of unspecified femur
+
anemias (D50-D64)
  
*'''[[Q72.41]]''' Longitudinal reduction defect of right femur
+
anemia of premature infant (P61.2)
  
*'''[[Q72.42]]''' Longitudinal reduction defect of left femur
+
benign (familial) polycythemia (D75.0)
  
*'''[[Q72.43]]''' Longitudinal reduction defect of femur, bilateral
+
congenital anemias (P61.2-P61.4)
  
*'''[[Q72.5]]''' Longitudinal reduction defect of tibia
+
newborn anemia due to isoimmunization (P55.-)
  
*'''[[Q72.50]]''' Longitudinal reduction defect of unspecified tibia
+
polycythemia neonatorum (P61.1)
  
*'''[[Q72.51]]''' Longitudinal reduction defect of right tibia
+
polycythemia NOS (D75.1)
  
*'''[[Q72.52]]''' Longitudinal reduction defect of left tibia
+
polycythemia vera (D45)
  
*'''[[Q72.53]]''' Longitudinal reduction defect of tibia, bilateral
+
secondary polycythemia (D75.1)
  
*'''[[Q72.6]]''' Longitudinal reduction defect of fibula
+
*'''[[R71.0]]''' Precipitous drop in hematocrit
  
*'''[[Q72.60]]''' Longitudinal reduction defect of unspecified fibula
+
Drop (precipitous) in hemoglobin
  
*'''[[Q72.61]]''' Longitudinal reduction defect of right fibula
+
Drop in hematocrit
  
*'''[[Q72.62]]''' Longitudinal reduction defect of left fibula
+
*'''[[R71.8]]''' Other abnormality of red blood cells
  
*'''[[Q72.63]]''' Longitudinal reduction defect of fibula, bilateral
+
Abnormal red-cell morphology NOS
  
*'''[[Q72.7]]''' Split foot
+
Abnormal red-cell volume NOS
  
*'''[[Q72.70]]''' Split foot, unspecified lower limb
+
Anisocytosis
  
*'''[[Q72.71]]''' Split foot, right lower limb
+
Poikilocytosis
  
*'''[[Q72.72]]''' Split foot, left lower limb
+
*'''[[R73]]''' Elevated blood glucose level
  
*'''[[Q72.73]]''' Split foot, bilateral
+
''Excludes1''  
  
*'''[[Q72.8]]''' Other reduction defects of lower limb
+
diabetes mellitus (E08-E13)
  
*'''[[Q72.81]]''' Congenital shortening of lower limb
+
diabetes mellitus in pregnancy, childbirth and the puerperium (O24.-)
  
*'''[[Q72.811]]''' Congenital shortening of right lower limb
+
neonatal disorders (P70.0-P70.2)
  
*'''[[Q72.812]]''' Congenital shortening of left lower limb
+
postsurgical hypoinsulinemia (E89.1)
  
*'''[[Q72.813]]''' Congenital shortening of lower limb, bilateral
+
*'''[[R73.0]]''' Abnormal glucose
  
*'''[[Q72.819]]''' Congenital shortening of unspecified lower limb
+
''Excludes1''  
  
*'''[[Q72.89]]''' Other reduction defects of lower limb
+
abnormal glucose in pregnancy (O99.81-)
  
*'''[[Q72.891]]''' Other reduction defects of right lower limb
+
diabetes mellitus (E08-E13)
  
*'''[[Q72.892]]''' Other reduction defects of left lower limb
+
dysmetabolic syndrome X (E88.81)
  
*'''[[Q72.893]]''' Other reduction defects of lower limb, bilateral
+
gestational diabetes (O24.4-)
  
*'''[[Q72.899]]''' Other reduction defects of unspecified lower limb
+
glycosuria (R81)
  
*'''[[Q72.9]]''' Unspecified reduction defect of lower limb
+
hypoglycemia (E16.2)
  
*'''[[Q72.90]]''' Unspecified reduction defect of unspecified lower limb
+
*'''[[R73.01]]''' Impaired fasting glucose
  
*'''[[Q72.91]]''' Unspecified reduction defect of right lower limb
+
Elevated fasting glucose
  
*'''[[Q72.92]]''' Unspecified reduction defect of left lower limb
+
*'''[[R73.02]]''' Impaired glucose tolerance (oral)
  
*'''[[Q72.93]]''' Unspecified reduction defect of lower limb, bilateral
+
Elevated glucose tolerance
  
*'''[[Q73]]''' Reduction defects of unspecified limb
+
*'''[[R73.03]]''' Prediabetes
  
*'''[[Q73.0]]''' Congenital absence of unspecified limb(s)
+
Latent diabetes
  
Amelia NOS
+
*'''[[R73.09]]''' Other abnormal glucose
  
*'''[[Q73.1]]''' Phocomelia, unspecified limb(s)
+
Abnormal glucose NOS
  
Phocomelia NOS
+
Abnormal non-fasting glucose tolerance
  
*'''[[Q73.8]]''' Other reduction defects of unspecified limb(s)
+
*'''[[R73.9]]''' Hyperglycemia, unspecified
  
Longitudinal reduction deformity of unspecified limb(s)
+
*'''[[R74]]''' Abnormal serum enzyme levels
  
Ectromelia of limb NOS
+
*'''[[R74.0]]''' Nonspecific elevation of levels of transaminase and lactic acid dehydrogenase (LDH)
  
Hemimelia of limb NOS
+
*'''[[R74.8]]''' Abnormal levels of other serum enzymes
  
Reduction defect of limb NOS
+
Abnormal level of acid phosphatase
  
*'''[[Q74]]''' Other congenital malformations of limb(s)
+
Abnormal level of alkaline phosphatase
  
''Excludes1''
+
Abnormal level of amylase
  
polydactyly (Q69.-)  
+
Abnormal level of lipase (triacylglycerol lipase)
  
reduction defect of limb (Q71-Q73)
+
*'''[[R74.9]]''' Abnormal serum enzyme level, unspecified
  
syndactyly (Q70.-)
+
*'''[[R75]]''' Inconclusive laboratory evidence of human immunodeficiency virus (HIV)
  
*'''[[Q74.0]]''' Other congenital malformations of upper limb(s), including shoulder girdle
+
Nonconclusive HIV-test finding in infants
  
Accessory carpal bones
+
''Excludes1''
  
Cleidocranial dysostosis
+
asymptomatic human immunodeficiency virus (HIV) infection status (Z21)
  
Congenital pseudarthrosis of clavicle
+
human immunodeficiency virus (HIV) disease (B20)
  
Macrodactylia (fingers)
+
*'''[[R76]]''' Other abnormal immunological findings in serum
  
Madelung's deformity
+
*'''[[R76.0]]''' Raised antibody titer
  
Radioulnar synostosis
+
''Excludes1''
  
Sprengel's deformity
+
isoimmunization in pregnancy (O36.0-O36.1)
  
Triphalangeal thumb
+
isoimmunization affecting newborn (P55.-)
  
*'''[[Q74.1]]''' Congenital malformation of knee
+
*'''[[R76.1]]''' Nonspecific reaction to test for tuberculosis
  
Congenital absence of patella
+
*'''[[R76.11]]''' Nonspecific reaction to tuberculin skin test without active tuberculosis
  
Congenital dislocation of patella
+
Abnormal result of Mantoux test
  
Congenital genu valgum
+
PPD positive
  
Congenital genu varum
+
Tuberculin (skin test) positive
  
Rudimentary patella
+
Tuberculin (skin test) reactor
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital dislocation of knee (Q68.2)
+
nonspecific reaction to cell mediated immunity measurement of gamma interferon antigen
 
 
congenital genu recurvatum (Q68.2)
 
 
 
nail patella syndrome (Q87.2)
 
  
*'''[[Q74.2]]''' Other congenital malformations of lower limb(s), including pelvic girdle
+
response without active tuberculosis (R76.12)
  
Congenital fusion of sacroiliac joint
+
*'''[[R76.12]]''' Nonspecific reaction to cell mediated immunity measurement of gamma interferon antigen
  
Congenital malformation of ankle joint
+
response without active tuberculosis
  
Congenital malformation of sacroiliac joint
+
Nonspecific reaction to QuantiFERON-TB test (QFT) without active tuberculosis
  
 
''Excludes1''  
 
''Excludes1''  
  
anteversion of femur (neck) (Q65.89)
+
nonspecific reaction to tuberculin skin test without active tuberculosis (R76.11)  
  
*'''[[Q74.3]]''' Arthrogryposis multiplex congenita
+
positive tuberculin skin test (R76.11)
  
*'''[[Q74.8]]''' Other specified congenital malformations of limb(s)
+
*'''[[R76.8]]''' Other specified abnormal immunological findings in serum
  
*'''[[Q74.9]]''' Unspecified congenital malformation of limb(s)
+
'''Raised level of immunoglobulins NOS'''
  
Congenital anomaly of limb(s) NOS
+
*'''[[R76.9]]''' Abnormal immunological finding in serum, unspecified
  
*'''[[Q75]]''' Other congenital malformations of skull and face bones
+
*'''[[R77]]''' Other abnormalities of plasma proteins
  
 
''Excludes1''  
 
''Excludes1''  
  
congenital malformation of face NOS (Q18.-)  
+
disorders of plasma-protein metabolism (E88.0-)
  
congenital malformation syndromes classified to Q87.-
+
*'''[[R77.0]]''' Abnormality of albumin
  
dentofacial anomalies (including malocclusion) (M26.-)
+
*'''[[R77.1]]''' Abnormality of globulin
  
musculoskeletal deformities of head and face (Q67.0-Q67.4)
+
Hyperglobulinemia NOS
  
skull defects associated with congenital anomalies of brain such as
+
*'''[[R77.2]]''' Abnormality of alphafetoprotein
  
anencephaly (Q00.0)
+
*'''[[R77.8]]''' Other specified abnormalities of plasma proteins
  
encephalocele (Q01.-)
+
*'''[[R77.9]]''' Abnormality of plasma protein, unspecified
  
hydrocephalus (Q03.-)
+
*'''[[R78]]''' Findings of drugs and other substances, not normally found in blood ''Use additional''
  
microcephaly (Q02)
+
code to identify the any retained foreign body, if applicable (Z18.-)  
  
*'''[[Q75.0]]''' Craniosynostosis
+
''Excludes1''  
  
Acrocephaly
+
mental or behavioral disorders due to psychoactive substance use (F10-F19)
  
Imperfect fusion of skull
+
*'''[[R78.0]]''' Finding of alcohol in blood ''Use additional''
  
Oxycephaly
+
external cause code (Y90.-), for detail regarding alcohol level
  
Trigonocephaly
+
*'''[[R78.1]]''' Finding of opiate drug in blood
  
*'''[[Q75.1]]''' Craniofacial dysostosis
+
*'''[[R78.2]]''' Finding of cocaine in blood
  
Crouzon's disease
+
*'''[[R78.3]]''' Finding of hallucinogen in blood
  
*'''[[Q75.2]]''' Hypertelorism
+
*'''[[R78.4]]''' Finding of other drugs of addictive potential in blood
  
*'''[[Q75.3]]''' Macrocephaly
+
*'''[[R78.5]]''' Finding of other psychotropic drug in blood
  
*'''[[Q75.4]]''' Mandibulofacial dysostosis
+
*'''[[R78.6]]''' Finding of steroid agent in blood
  
Franceschetti syndrome
+
*'''[[R78.7]]''' Finding of abnormal level of heavy metals in blood
  
Treacher Collins syndrome
+
*'''[[R78.71]]''' Abnormal lead level in blood
  
*'''[[Q75.5]]''' Oculomandibular dysostosis
+
''Excludes1''  
  
*'''[[Q75.8]]''' Other specified congenital malformations of skull and face bones
+
lead poisoning (T56.0-)
  
Absence of skull bone, congenital
+
*'''[[R78.79]]''' Finding of abnormal level of heavy metals in blood
  
Congenital deformity of forehead
+
*'''[[R78.8]]''' Finding of other specified substances, not normally found in blood
  
Platybasia
+
*'''[[R78.81]]''' Bacteremia
  
*'''[[Q75.9]]''' Congenital malformation of skull and face bones, unspecified
+
''Excludes1''  
  
Congenital anomaly of face bones NOS
+
sepsis-code to specified infection
  
Congenital anomaly of skull NOS
+
*'''[[R78.89]]''' Finding of other specified substances, not normally found in blood
  
*'''[[Q76]]''' Congenital malformations of spine and bony thorax
+
Finding of abnormal level of lithium in blood
  
''Excludes1''  
+
*'''[[R78.9]]''' Finding of unspecified substance, not normally found in blood
  
congenital musculoskeletal deformities of spine and chest (Q67.5-Q67.8)
+
*'''[[R79]]''' Other abnormal findings of blood chemistry ''Use additional''
  
*'''[[Q76.0]]''' Spina bifida occulta
+
code to identify any retained foreign body, if applicable (Z18.-)
  
 
''Excludes1''  
 
''Excludes1''  
  
meningocele (spinal) (Q05.-)  
+
asymptomatic hyperuricemia (E79.0)  
  
spina bifida (aperta) (cystica) (Q05.-)
+
hyperglycemia NOS (R73.9)  
  
*'''[[Q76.1]]''' Klippel-Feil syndrome
+
hypoglycemia NOS (E16.2)
  
Cervical fusion syndrome
+
neonatal hypoglycemia (P70.3-P70.4)
  
*'''[[Q76.2]]''' Congenital spondylolisthesis
+
specific findings indicating disorder of amino-acid metabolism (E70-E72)
  
Congenital spondylolysis
+
specific findings indicating disorder of carbohydrate metabolism (E73-E74)
  
''Excludes1''
+
specific findings indicating disorder of lipid metabolism (E75.-)
  
spondylolisthesis (acquired) (M43.1-)
+
*'''[[R79.0]]''' Abnormal level of blood mineral
  
spondylolysis (acquired) (M43.0-)
+
Abnormal blood level of cobalt
  
*'''[[Q76.3]]''' Congenital scoliosis due to congenital bony malformation
+
Abnormal blood level of copper
  
Hemivertebra fusion or failure of segmentation with scoliosis
+
Abnormal blood level of iron
  
*'''[[Q76.4]]''' Other congenital malformations of spine, not associated with scoliosis
+
Abnormal blood level of magnesium
  
*'''[[Q76.41]]''' Congenital kyphosis
+
Abnormal blood level of mineral NEC
  
*'''[[Q76.411]]''' Congenital kyphosis, occipito-atlanto-axial region
+
Abnormal blood level of zinc
  
*'''[[Q76.412]]''' Congenital kyphosis, cervical region
+
''Excludes1''  
  
*'''[[Q76.413]]''' Congenital kyphosis, cervicothoracic region
+
abnormal level of lithium (R78.89)
  
*'''[[Q76.414]]''' Congenital kyphosis, thoracic region
+
disorders of mineral metabolism (E83.-)
  
*'''[[Q76.415]]''' Congenital kyphosis, thoracolumbar region
+
neonatal hypomagnesemia (P71.2)
  
*'''[[Q76.419]]''' Congenital kyphosis, unspecified region
+
nutritional mineral deficiency (E58-E61)
  
*'''[[Q76.42]]''' Congenital lordosis
+
*'''[[R79.1]]''' Abnormal coagulation profile
  
*'''[[Q76.425]]''' Congenital lordosis, thoracolumbar region
+
Abnormal or prolonged bleeding time
  
*'''[[Q76.426]]''' Congenital lordosis, lumbar region
+
Abnormal or prolonged coagulation time
  
*'''[[Q76.427]]''' Congenital lordosis, lumbosacral region
+
Abnormal or prolonged partial thromboplastin time (PTT)
  
*'''[[Q76.428]]''' Congenital lordosis, sacral and sacrococcygeal region
+
Abnormal or prolonged prothrombin time (PT)
  
*'''[[Q76.429]]''' Congenital lordosis, unspecified region
+
''Excludes1''  
  
*'''[[Q76.49]]''' Other congenital malformations of spine, not associated with scoliosis
+
coagulation defects (D68.-)
  
Congenital absence of vertebra NOS
+
''Excludes2''
  
Congenital fusion of spine NOS
+
abnormality of fluid, electrolyte or acid-base balance (E86-E87)
  
Congenital malformation of lumbosacral (joint) (region) NOS
+
*'''[[R79.8]]''' Other specified abnormal findings of blood chemistry
  
Congenital malformation of spine NOS
+
*'''[[R79.81]]''' Abnormal blood-gas level
  
Hemivertebra NOS
+
*'''[[R79.82]]''' Elevated C-reactive protein (CRP)
  
Malformation of spine NOS
+
*'''[[R79.89]]''' Other specified abnormal findings of blood chemistry
  
Platyspondylisis NOS
+
*'''[[R79.9]]''' Abnormal finding of blood chemistry, unspecified
  
Supernumerary vertebra NOS
+
Abnormal findings on examination of urine, without diagnosis (R80-R82)
  
*'''[[Q76.5]]''' Cervical rib
+
''Excludes1''  
 
 
Supernumerary rib in cervical region
 
  
*'''[[Q76.6]]''' Other congenital malformations of ribs
+
abnormal findings on antenatal screening of mother (O28.-)
  
Accessory rib
+
diagnostic abnormal findings classified elsewhere - see Alphabetical Index
  
Congenital absence of rib
+
specific findings indicating disorder of amino-acid metabolism (E70-E72)
  
Congenital fusion of ribs
+
specific findings indicating disorder of carbohydrate metabolism (E73-E74)
  
Congenital malformation of ribs NOS
+
*'''[[R80]]''' Proteinuria
  
 
''Excludes1''  
 
''Excludes1''  
  
short rib syndrome (Q77.2)
+
gestational proteinuria (O12.1-)
  
*'''[[Q76.7]]''' Congenital malformation of sternum
+
*'''[[R80.0]]''' Isolated proteinuria
  
Congenital absence of sternum
+
Idiopathic proteinuria
  
Sternum bifidum
+
''Excludes1''
  
*'''[[Q76.8]]''' Other congenital malformations of bony thorax
+
isolated proteinuria with specific morphological lesion (N06.-)
  
*'''[[Q76.9]]''' Congenital malformation of bony thorax, unspecified
+
*'''[[R80.1]]''' Persistent proteinuria, unspecified
  
*'''[[Q77]]''' Osteochondrodysplasia with defects of growth of tubular bones and spine
+
*'''[[R80.2]]''' Orthostatic proteinuria, unspecified
  
''Excludes1''
+
Postural proteinuria
  
mucopolysaccharidosis (E76.0-E76.3)
+
*'''[[R80.3]]''' Bence Jones proteinuria
  
''Excludes2''  
+
*'''[[R80.8]]''' Other proteinuria
  
congenital myotonic chondrodystrophy (G71.13)
+
*'''[[R80.9]]''' Proteinuria, unspecified
  
*'''[[Q77.0]]''' Achondrogenesis
+
Albuminuria NOS
  
Hypochondrogenesis
+
*'''[[R81]]''' Glycosuria
  
*'''[[Q77.1]]''' Thanatophoric short stature
+
''Excludes1''  
  
*'''[[Q77.2]]''' Short rib syndrome
+
renal glycosuria (E74.8)
  
Asphyxiating thoracic dysplasia (Jeune)
+
*'''[[R82]]''' Other and unspecified abnormal findings in urine
  
*'''[[Q77.3]]''' Chondrodysplasia punctata
+
''Includes''  
  
''Excludes1''
+
chromoabnormalities in urine ''Use additional''  
  
Rhizomelic chondrodysplasia punctata (E71.43)
+
code to identify any retained foreign body, if applicable (Z18.-)  
  
*'''[[Q77.4]]''' Achondroplasia
+
''Excludes2''  
  
Hypochondroplasia
+
hematuria (R31.-)
  
Osteosclerosis congenita
+
*'''[[R82.0]]''' Chyluria
  
*'''[[Q77.5]]''' Diastrophic dysplasia
+
''Excludes1''  
  
*'''[[Q77.6]]''' Chondroectodermal dysplasia
+
filarial chyluria (B74.-)
  
Ellis-van Creveld syndrome
+
*'''[[R82.1]]''' Myoglobinuria
  
*'''[[Q77.7]]''' Spondyloepiphyseal dysplasia
+
*'''[[R82.2]]''' Biliuria
  
*'''[[Q77.8]]''' Other osteochondrodysplasia with defects of growth of tubular bones and spine
+
*'''[[R82.3]]''' Hemoglobinuria
  
*'''[[Q77.9]]''' Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
+
''Excludes1''  
  
*'''[[Q78]]''' Other osteochondrodysplasias
+
hemoglobinuria due to hemolysis from external causes NEC (D59.6)
  
''Excludes2''
+
hemoglobinuria due to paroxysmal nocturnal (Marchiafava-Micheli) (D59.5)
  
congenital myotonic chondrodystrophy (G71.13)
+
*'''[[R82.4]]''' Acetonuria
  
*'''[[Q78.0]]''' Osteogenesis imperfecta
+
Ketonuria
  
Fragilitas ossium
+
*'''[[R82.5]]''' Elevated urine levels of drugs, medicaments and biological substances
  
Osteopsathyrosis
+
Elevated urine levels of catecholamines
  
*'''[[Q78.1]]''' Polyostotic fibrous dysplasia
+
Elevated urine levels of indoleacetic acid
  
Albright(-McCune)(-Sternberg) syndrome
+
Elevated urine levels of 17-ketosteroids
  
*'''[[Q78.2]]''' Osteopetrosis
+
Elevated urine levels of steroids
  
Albers-Schönberg syndrome
+
*'''[[R82.6]]''' Abnormal urine levels of substances chiefly nonmedicinal as to source
  
Osteosclerosis NOS
+
Abnormal urine level of heavy metals
  
*'''[[Q78.3]]''' Progressive diaphyseal dysplasia
+
*'''[[R82.7]]''' Abnormal findings on microbiological examination of urine
  
Camurati-Engelmann syndrome
+
''Excludes1''
  
*'''[[Q78.4]]''' Enchondromatosis
+
colonization status (Z22.-)
  
Maffucci's syndrome
+
*'''[[R82.71]]''' Bacteriuria
  
Ollier's disease
+
*'''[[R82.79]]''' Other abnormal findings on microbiological examination of urine
  
*'''[[Q78.5]]''' Metaphyseal dysplasia
+
Positive culture findings of urine
  
Pyle's syndrome
+
*'''[[R82.8]]''' Abnormal findings on cytological and histological examination of urine
  
*'''[[Q78.6]]''' Multiple congenital exostoses
+
*'''[[R82.81]]''' Pyuria
  
Diaphyseal aclasis
+
Sterile pyuria
  
*'''[[Q78.8]]''' Other specified osteochondrodysplasias
+
*'''[[R82.89]]''' Other abnormal findings on cytological and histological examination of urine
  
Osteopoikilosis
+
*'''[[R82.9]]''' Other and unspecified abnormal findings in urine
  
*'''[[Q78.9]]''' Osteochondrodysplasia, unspecified
+
*'''[[R82.90]]''' Unspecified abnormal findings in urine
  
Chondrodystrophy NOS
+
*'''[[R82.91]]''' Other chromoabnormalities of urine
  
Osteodystrophy NOS
+
Chromoconversion (dipstick)
  
*'''[[Q79]]''' Congenital malformations of musculoskeletal system, not elsewhere classified
+
Idiopathic dipstick converts positive for blood with no cellular forms in sediment
  
''Excludes2''  
+
''Excludes1''  
  
congenital (sternomastoid) torticollis (Q68.0)
+
hemoglobinuria (R82.3)  
  
*'''[[Q79.0]]''' Congenital diaphragmatic hernia
+
myoglobinuria (R82.1)
  
''Excludes1''  
+
*'''[[R82.99]]''' Other abnormal findings in urine
  
congenital hiatus hernia (Q40.1)
+
*'''[[R82.991]]''' Hypocitraturia
  
*'''[[Q79.1]]''' Other congenital malformations of diaphragm
+
*'''[[R82.992]]''' Hyperoxaluria
  
Absence of diaphragm
+
''Excludes1''
  
Congenital malformation of diaphragm NOS
+
Primary hyperoxaluria (E72.53)
  
Eventration of diaphragm
+
*'''[[R82.993]]''' Hyperuricosuria
  
*'''[[Q79.2]]''' Exomphalos
+
*'''[[R82.994]]''' Hypercalciuria
  
Omphalocele
+
Idiopathic hypercalciuria
  
''Excludes1''  
+
*'''[[R82.998]]''' Other abnormal findings in urine
  
umbilical hernia (K42.-)
+
Cells and casts in urine
  
*'''[[Q79.3]]''' Gastroschisis
+
Crystalluria
  
*'''[[Q79.4]]''' Prune belly syndrome
+
Melanuria
  
Congenital prolapse of bladder mucosa
+
Abnormal findings on examination of other body fluids, substances and tissues, without diagnosis (R83-R89)
  
Eagle-Barrett syndrome
+
''Excludes1''
  
*'''[[Q79.5]]''' Other congenital malformations of abdominal wall
+
abnormal findings on antenatal screening of mother (O28.-)
  
''Excludes1''
+
diagnostic abnormal findings classified elsewhere - see Alphabetical Index
  
umbilical hernia (K42.-)
+
''Excludes2''
  
*'''[[Q79.51]]''' Congenital hernia of bladder
+
abnormal findings on examination of blood, without diagnosis (R70-R79)
  
*'''[[Q79.59]]''' Other congenital malformations of abdominal wall
+
abnormal findings on examination of urine, without diagnosis (R80-R82)
  
*'''[[Q79.6]]''' Ehlers-Danlos syndromes
+
abnormal tumor markers (R97.-)
  
*'''[[Q79.60]]''' Ehlers-Danlos syndrome, unspecified
+
*'''[[R83]]''' Abnormal findings in cerebrospinal fluid
  
*'''[[Q79.61]]''' Classical Ehlers-Danlos syndrome
+
*'''[[R83.0]]''' Abnormal level of enzymes in cerebrospinal fluid
  
Classical EDS (cEDS)
+
*'''[[R83.1]]''' Abnormal level of hormones in cerebrospinal fluid
  
*'''[[Q79.62]]''' Hypermobile Ehlers-Danlos syndrome
+
*'''[[R83.2]]''' Abnormal level of other drugs, medicaments and biological substances in cerebrospinal fluid
  
Hypermobile EDS (hEDS)
+
*'''[[R83.3]]''' Abnormal level of substances chiefly nonmedicinal as to source in cerebrospinal fluid
  
*'''[[Q79.63]]''' Vascular Ehlers-Danlos syndrome
+
*'''[[R83.4]]''' Abnormal immunological findings in cerebrospinal fluid
  
Vascular EDS (vEDS)
+
*'''[[R83.5]]''' Abnormal microbiological findings in cerebrospinal fluid
  
*'''[[Q79.69]]''' Other Ehlers-Danlos syndromes
+
Positive culture findings in cerebrospinal fluid
  
*'''[[Q79.8]]''' Other congenital malformations of musculoskeletal system
+
''Excludes1''  
  
Absence of muscle
+
colonization status (Z22.-)
  
Absence of tendon
+
*'''[[R83.6]]''' Abnormal cytological findings in cerebrospinal fluid
  
Accessory muscle
+
*'''[[R83.8]]''' Other abnormal findings in cerebrospinal fluid
  
Amyotrophia congenita
+
Abnormal chromosomal findings in cerebrospinal fluid
  
Congenital constricting bands
+
*'''[[R83.9]]''' Unspecified abnormal finding in cerebrospinal fluid
  
Congenital shortening of tendon
+
*'''[[R84]]''' Abnormal findings in specimens from respiratory organs and thorax
  
Poland syndrome
+
''Includes''
  
*'''[[Q79.9]]''' Congenital malformation of musculoskeletal system, unspecified
+
abnormal findings in bronchial washings
  
Congenital anomaly of musculoskeletal system NOS
+
abnormal findings in nasal secretions
  
Congenital deformity of musculoskeletal system NOS
+
abnormal findings in pleural fluid
  
Other congenital malformations (Q80-Q89)
+
abnormal findings in sputum
  
*'''[[Q80]]''' Congenital ichthyosis
+
abnormal findings in throat scrapings
  
''Excludes1''
+
''Excludes1''  
 
 
Refsum's disease (G60.1)
 
  
*'''[[Q80.0]]''' Ichthyosis vulgaris
+
blood-stained sputum (R04.2)
  
*'''[[Q80.1]]''' X-linked ichthyosis
+
*'''[[R84.0]]''' Abnormal level of enzymes in specimens from respiratory organs and thorax
  
*'''[[Q80.2]]''' Lamellar ichthyosis
+
*'''[[R84.1]]''' Abnormal level of hormones in specimens from respiratory organs and thorax
  
Collodion baby
+
*'''[[R84.2]]''' Abnormal level of other drugs, medicaments and biological substances in specimens from respiratory
  
*'''[[Q80.3]]''' Congenital bullous ichthyosiform erythroderma
+
organs and thorax
  
*'''[[Q80.4]]''' Harlequin fetus
+
*'''[[R84.3]]''' Abnormal level of substances chiefly nonmedicinal as to source in specimens from respiratory organs
  
*'''[[Q80.8]]''' Other congenital ichthyosis
+
and thorax
  
*'''[[Q80.9]]''' Congenital ichthyosis, unspecified
+
*'''[[R84.4]]''' Abnormal immunological findings in specimens from respiratory organs and thorax
  
*'''[[Q81]]''' Epidermolysis bullosa
+
*'''[[R84.5]]''' Abnormal microbiological findings in specimens from respiratory organs and thorax
  
*'''[[Q81.0]]''' Epidermolysis bullosa simplex
+
Positive culture findings in specimens from respiratory organs and thorax
  
 
''Excludes1''  
 
''Excludes1''  
  
Cockayne's syndrome (Q87.19)
+
colonization status (Z22.-)
  
*'''[[Q81.1]]''' Epidermolysis bullosa letalis
+
*'''[[R84.6]]''' Abnormal cytological findings in specimens from respiratory organs and thorax
  
Herlitz' syndrome
+
*'''[[R84.7]]''' Abnormal histological findings in specimens from respiratory organs and thorax
  
*'''[[Q81.2]]''' Epidermolysis bullosa dystrophica
+
*'''[[R84.8]]''' Other abnormal findings in specimens from respiratory organs and thorax
  
*'''[[Q81.8]]''' Other epidermolysis bullosa
+
Abnormal chromosomal findings in specimens from respiratory organs and thorax
  
*'''[[Q81.9]]''' Epidermolysis bullosa, unspecified
+
*'''[[R84.9]]''' Unspecified abnormal finding in specimens from respiratory organs and thorax
  
*'''[[Q82]]''' Other congenital malformations of skin
+
*'''[[R85]]''' Abnormal findings in specimens from digestive organs and abdominal cavity
  
''Excludes1''  
+
''Includes''  
  
acrodermatitis enteropathica (E83.2)
+
abnormal findings in peritoneal fluid
  
congenital erythropoietic porphyria (E80.0)
+
abnormal findings in saliva
  
pilonidal cyst or sinus (L05.-)
+
''Excludes1''
  
Sturge-Weber (-Dimitri) syndrome (Q85.8)
+
cloudy peritoneal dialysis effluent (R88.0)  
  
*'''[[Q82.0]]''' Hereditary lymphedema
+
fecal abnormalities (R19.5)
  
*'''[[Q82.1]]''' Xeroderma pigmentosum
+
*'''[[R85.0]]''' Abnormal level of enzymes in specimens from digestive organs and abdominal cavity
  
*'''[[Q82.2]]''' Congenital cutaneous mastocytosis
+
*'''[[R85.1]]''' Abnormal level of hormones in specimens from digestive organs and abdominal cavity
  
Congenital diffuse cutaneous mastocytosis
+
*'''[[R85.2]]''' Abnormal level of other drugs, medicaments and biological substances in specimens from digestive
  
Congenital maculopapular cutaneous mastocytosis
+
organs and abdominal cavity
  
Congenital urticaria pigmentosa
+
*'''[[R85.3]]''' Abnormal level of substances chiefly nonmedicinal as to source in specimens from digestive organs
  
''Excludes1''
+
and abdominal cavity
  
cutaneous mastocytosis NOS (D47.01)
+
*'''[[R85.4]]''' Abnormal immunological findings in specimens from digestive organs and abdominal cavity
  
diffuse cutaneous mastocytosis (with onset after newborn period) (D47.01)
+
*'''[[R85.5]]''' Abnormal microbiological findings in specimens from digestive organs and abdominal cavity
  
malignant mastocytosis (C96.2-)
+
Positive culture findings in specimens from digestive organs and abdominal cavity
  
systemic mastocytosis (D47.02)
+
''Excludes1''
  
urticaria pigmentosa (non-congenital) (with onset after newborn period) (D47.01)
+
colonization status (Z22.-)
  
*'''[[Q82.3]]''' Incontinentia pigmenti
+
*'''[[R85.6]]''' Abnormal cytological findings in specimens from digestive organs and abdominal cavity
  
*'''[[Q82.4]]''' Ectodermal dysplasia (anhidrotic)
+
*'''[[R85.61]]''' Abnormal cytologic smear of anus
  
 
''Excludes1''  
 
''Excludes1''  
  
Ellis-van Creveld syndrome (Q77.6)
+
abnormal cytological findings in specimens from other digestive organs and abdominal
 
 
*'''[[Q82.5]]''' Congenital non-neoplastic nevus
 
  
Birthmark NOS
+
cavity (R85.69)
  
Flammeus Nevus
+
carcinoma in situ of anus (histologically confirmed) (D01.3)
  
Portwine Nevus
+
anal intraepithelial neoplasia I (AIN I) (K62.82)
  
Sanguineous Nevus
+
anal intraepithelial neoplasia II (AIN II) (K62.82)
  
Strawberry Nevus
+
anal intraepithelial neoplasia III (AIN III) (D01.3)
  
Vascular Nevus NOS
+
dysplasia (mild) (moderate) of anus (histologically confirmed) (K62.82)
  
Verrucous Nevus
+
severe dysplasia of anus (histologically confirmed) (D01.3)
  
 
''Excludes2''  
 
''Excludes2''  
  
Café au lait spots (L81.3)
+
anal high risk human papillomavirus (HPV) DNA test positive (R85.81)  
 
 
lentigo (L81.4)  
 
 
 
nevus NOS (D22.-)  
 
  
araneus nevus (I78.1)  
+
anal low risk human papillomavirus (HPV) DNA test positive (R85.82)
  
melanocytic nevus (D22.-)
+
*'''[[R85.610]]''' Atypical squamous cells of undetermined significance on cytologic smear of anus
  
pigmented nevus (D22.-)  
+
(ASC-US)
  
spider nevus (I78.1)
+
*'''[[R85.611]]''' Atypical squamous cells cannot exclude high grade squamous intraepithelial lesion on
  
stellar nevus (I78.1)
+
cytologic smear of anus (ASC-H)
  
*'''[[Q82.6]]''' Congenital sacral dimple
+
*'''[[R85.612]]''' Low grade squamous intraepithelial lesion on cytologic smear of anus (LGSIL)
  
Parasacral dimple
+
*'''[[R85.613]]''' High grade squamous intraepithelial lesion on cytologic smear of anus (HGSIL)
  
''Excludes2''  
+
*'''[[R85.614]]''' Cytologic evidence of malignancy on smear of anus
  
pilonidal cyst with abscess (L05.01)
+
*'''[[R85.615]]''' Unsatisfactory cytologic smear of anus
  
pilonidal cyst without abscess (L05.91)
+
Inadequate sample of cytologic smear of anus
  
*'''[[Q82.8]]''' Other specified congenital malformations of skin
+
*'''[[R85.616]]''' Satisfactory anal smear but lacking transformation zone
  
Abnormal palmar creases
+
*'''[[R85.618]]''' Other abnormal cytological findings on specimens from anus
  
Accessory skin tags
+
*'''[[R85.619]]''' Unspecified abnormal cytological findings in specimens from anus
  
Benign familial pemphigus (Hailey-Hailey)
+
Abnormal anal cytology NOS
  
Congenital poikiloderma
+
Atypical glandular cells of anus NOS
  
Cutis laxa (hyperelastica)
+
*'''[[R85.69]]''' Abnormal cytological findings in specimens from other digestive organs and abdominal cavity
  
Dermatoglyphic anomalies
+
*'''[[R85.7]]''' Abnormal histological findings in specimens from digestive organs and abdominal cavity
  
Inherited keratosis palmaris et plantaris
+
*'''[[R85.8]]''' Other abnormal findings in specimens from digestive organs and abdominal cavity
  
Keratosis follicularis (Darier-White)  
+
*'''[[R85.81]]''' Anal high risk human papillomavirus (HPV) DNA test positive
  
 
''Excludes1''  
 
''Excludes1''  
  
Ehlers-Danlos syndrome (Q79.6-)
+
anogenital warts due to human papillomavirus (HPV) (A63.0)  
  
*'''[[Q82.9]]''' Congenital malformation of skin, unspecified
+
condyloma acuminatum (A63.0)
  
*'''[[Q83]]''' Congenital malformations of breast
+
*'''[[R85.82]]''' Anal low risk human papillomavirus (HPV) DNA test positive ''Use additional''
  
''Excludes2''
+
code for associated human papillomavirus (B97.7)
  
absence of pectoral muscle (Q79.8)
+
*'''[[R85.89]]''' Other abnormal findings in specimens from digestive organs and abdominal cavity
  
hypoplasia of breast (N64.82)
+
Abnormal chromosomal findings in specimens from digestive organs and abdominal cavity
  
micromastia (N64.82)
+
*'''[[R85.9]]''' Unspecified abnormal finding in specimens from digestive organs and abdominal cavity
  
*'''[[Q83.0]]''' Congenital absence of breast with absent nipple
+
*'''[[R86]]''' Abnormal findings in specimens from male genital organs
  
*'''[[Q83.1]]''' Accessory breast
+
''Includes''  
  
Supernumerary breast
+
abnormal findings in prostatic secretions
  
*'''[[Q83.2]]''' Absent nipple
+
abnormal findings in semen, seminal fluid
  
*'''[[Q83.3]]''' Accessory nipple
+
abnormal spermatozoa
  
Supernumerary nipple
+
''Excludes1''
  
*'''[[Q83.8]]''' Other congenital malformations of breast
+
azoospermia (N46.0-)
  
*'''[[Q83.9]]''' Congenital malformation of breast, unspecified
+
oligospermia (N46.1-)
  
*'''[[Q84]]''' Other congenital malformations of integument
+
*'''[[R86.0]]''' Abnormal level of enzymes in specimens from male genital organs
  
*'''[[Q84.0]]''' Congenital alopecia
+
*'''[[R86.1]]''' Abnormal level of hormones in specimens from male genital organs
  
Congenital atrichosis
+
*'''[[R86.2]]''' Abnormal level of other drugs, medicaments and biological substances in specimens from male
  
*'''[[Q84.1]]''' Congenital morphological disturbances of hair, not elsewhere classified
+
genital organs
  
Beaded hair
+
*'''[[R86.3]]''' Abnormal level of substances chiefly nonmedicinal as to source in specimens from male genital
  
Monilethrix
+
organs
  
Pili annulati
+
*'''[[R86.4]]''' Abnormal immunological findings in specimens from male genital organs
  
''Excludes1''
+
*'''[[R86.5]]''' Abnormal microbiological findings in specimens from male genital organs
  
Menkes' kinky hair syndrome (E83.0)
+
Positive culture findings in specimens from male genital organs
  
*'''[[Q84.2]]''' Other congenital malformations of hair
+
''Excludes1''  
  
Congenital hypertrichosis
+
colonization status (Z22.-)
  
Congenital malformation of hair NOS
+
*'''[[R86.6]]''' Abnormal cytological findings in specimens from male genital organs
  
Persistent lanugo
+
*'''[[R86.7]]''' Abnormal histological findings in specimens from male genital organs
  
*'''[[Q84.3]]''' Anonychia
+
*'''[[R86.8]]''' Other abnormal findings in specimens from male genital organs
  
''Excludes1''
+
Abnormal chromosomal findings in specimens from male genital organs
  
nail patella syndrome (Q87.2)
+
*'''[[R86.9]]''' Unspecified abnormal finding in specimens from male genital organs
  
*'''[[Q84.4]]''' Congenital leukonychia
+
*'''[[R87]]''' Abnormal findings in specimens from female genital organs
  
*'''[[Q84.5]]''' Enlarged and hypertrophic nails
+
''Includes''  
  
Congenital onychauxis
+
abnormal findings in secretion and smears from cervix uteri
  
Pachyonychia
+
abnormal findings in secretion and smears from vagina
  
*'''[[Q84.6]]''' Other congenital malformations of nails
+
abnormal findings in secretion and smears from vulva
  
Congenital clubnail
+
*'''[[R87.0]]''' Abnormal level of enzymes in specimens from female genital organs
  
Congenital koilonychia
+
*'''[[R87.1]]''' Abnormal level of hormones in specimens from female genital organs
  
Congenital malformation of nail NOS
+
*'''[[R87.2]]''' Abnormal level of other drugs, medicaments and biological substances in specimens from female
  
*'''[[Q84.8]]''' Other specified congenital malformations of integument
+
genital organs
  
Aplasia cutis congenita
+
*'''[[R87.3]]''' Abnormal level of substances chiefly nonmedicinal as to source in specimens from female genital
  
*'''[[Q84.9]]''' Congenital malformation of integument, unspecified
+
organs
  
Congenital anomaly of integument NOS
+
*'''[[R87.4]]''' Abnormal immunological findings in specimens from female genital organs
  
Congenital deformity of integument NOS
+
*'''[[R87.5]]''' Abnormal microbiological findings in specimens from female genital organs
  
*'''[[Q85]]''' Phakomatoses, not elsewhere classified
+
Positive culture findings in specimens from female genital organs
  
 
''Excludes1''  
 
''Excludes1''  
  
ataxia telangiectasia (Louis-Bar) (G11.3)  
+
colonization status (Z22.-)
  
familial dysautonomia (Riley-Day) (G90.1)
+
*'''[[R87.6]]''' Abnormal cytological findings in specimens from female genital organs
  
*'''[[Q85.0]]''' Neurofibromatosis (nonmalignant)
+
*'''[[R87.61]]''' Abnormal cytological findings in specimens from cervix uteri
  
*'''[[Q85.00]]''' Neurofibromatosis, unspecified
+
''Excludes1''  
  
*'''[[Q85.01]]''' Neurofibromatosis, type 1
+
abnormal cytological findings in specimens from other female genital organs (R87.69)
  
Von Recklinghausen disease
+
abnormal cytological findings in specimens from vagina (R87.62-)
  
*'''[[Q85.02]]''' Neurofibromatosis, type 2
+
carcinoma in situ of cervix uteri (histologically confirmed) (D06.-)
  
Acoustic neurofibromatosis
+
cervical intraepithelial neoplasia I (CIN I) (N87.0)
  
*'''[[Q85.03]]''' Schwannomatosis
+
cervical intraepithelial neoplasia II (CIN II) (N87.1)
  
*'''[[Q85.09]]''' Other neurofibromatosis
+
cervical intraepithelial neoplasia III (CIN III) (D06.-)
  
*'''[[Q85.1]]''' Tuberous sclerosis
+
dysplasia (mild) (moderate) of cervix uteri (histologically confirmed) (N87.-)
  
Bourneville's disease
+
severe dysplasia of cervix uteri (histologically confirmed) (D06.-)
  
Epiloia
+
''Excludes2''
  
*'''[[Q85.8]]''' Other phakomatoses, not elsewhere classified
+
cervical high risk human papillomavirus (HPV) DNA test positive (R87.810)
  
Peutz-Jeghers Syndrome
+
cervical low risk human papillomavirus (HPV) DNA test positive (R87.820)
  
Sturge-Weber(-Dimitri) syndrome
+
*'''[[R87.610]]''' Atypical squamous cells of undetermined significance on cytologic smear of cervix
  
von Hippel-Lindau syndrome
+
(ASC-US)
  
''Excludes1''
+
*'''[[R87.611]]''' Atypical squamous cells cannot exclude high grade squamous intraepithelial lesion on
  
Meckel-Gruber syndrome (Q61.9)
+
cytologic smear of cervix (ASC-H)
  
*'''[[Q85.9]]''' Phakomatosis, unspecified
+
*'''[[R87.612]]''' Low grade squamous intraepithelial lesion on cytologic smear of cervix (LGSIL)
  
Hamartosis NOS
+
*'''[[R87.613]]''' High grade squamous intraepithelial lesion on cytologic smear of cervix (HGSIL)
  
*'''[[Q86]]''' Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
+
*'''[[R87.614]]''' Cytologic evidence of malignancy on smear of cervix
  
''Excludes2''  
+
*'''[[R87.615]]''' Unsatisfactory cytologic smear of cervix
  
iodine-deficiency-related hypothyroidism (E00-E02)
+
Inadequate sample of cytologic smear of cervix
  
nonteratogenic effects of substances transmitted via placenta or breast milk (P04.-)
+
*'''[[R87.616]]''' Satisfactory cervical smear but lacking transformation zone
  
*'''[[Q86.0]]''' Fetal alcohol syndrome (dysmorphic)
+
*'''[[R87.618]]''' Other abnormal cytological findings on specimens from cervix uteri
  
*'''[[Q86.1]]''' Fetal hydantoin syndrome
+
*'''[[R87.619]]''' Unspecified abnormal cytological findings in specimens from cervix uteri
  
Meadow's syndrome
+
Abnormal cervical cytology NOS
  
*'''[[Q86.2]]''' Dysmorphism due to warfarin
+
Abnormal Papanicolaou smear of cervix NOS
  
*'''[[Q86.8]]''' Other congenital malformation syndromes due to known exogenous causes
+
Abnormal thin preparation smear of cervix NOS
  
*'''[[Q87]]''' Other specified congenital malformation syndromes affecting multiple systems ''Use additional''
+
Atypical endocervial cells of cervix NOS
  
code(s) to identify all associated manifestations
+
Atypical endometrial cells of cervix NOS
  
*'''[[Q87.0]]''' Congenital malformation syndromes predominantly affecting facial appearance
+
Atypical glandular cells of cervix NOS
  
Acrocephalopolysyndactyly
+
*'''[[R87.62]]''' Abnormal cytological findings in specimens from vagina ''Use additional''
  
Acrocephalosyndactyly (Apert)  
+
code to identify acquired absence of uterus and cervix, if applicable (Z90.71-)  
  
Cryptophthalmos syndrome
+
''Excludes1''
  
Cyclopia
+
abnormal cytological findings in specimens from cervix uteri (R87.61-)
  
Goldenhar syndrome
+
abnormal cytological findings in specimens from other female genital organs (R87.69)
  
Moebius syndrome
+
carcinoma in situ of vagina (histologically confirmed) (D07.2)
  
Oro-facial-digital syndrome
+
vaginal intraepithelial neoplasia I (VAIN I) (N89.0)
  
Robin syndrome
+
vaginal intraepithelial neoplasia II (VAIN II) (N89.1)
  
Whistling face
+
vaginal intraepithelial neoplasia III (VAIN III) (D07.2)
  
*'''[[Q87.1]]''' Congenital malformation syndromes predominantly associated with short stature
+
dysplasia (mild) (moderate) of vagina (histologically confirmed) (N89.-)
  
''Excludes1''
+
severe dysplasia of vagina (histologically confirmed) (D07.2)
  
Ellis-van Creveld syndrome (Q77.6)
+
''Excludes2''
  
Smith-Lemli-Opitz syndrome (E78.72)
+
vaginal high risk human papillomavirus (HPV) DNA test positive (R87.811)  
  
*'''[[Q87.11]]''' Prader-Willi syndrome
+
vaginal low risk human papillomavirus (HPV) DNA test positive (R87.821)
  
*'''[[Q87.19]]''' Other congenital malformation syndromes predominantly associated with short stature
+
*'''[[