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Category:Genodermatoses
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Pages in category "Genodermatoses"
The following 166 pages are in this category, out of 166 total.
A
- Acne vermoulanti
- Acral peeling skin syndrome
- Acrokeratosis verruciformis of Hopf
- Acrokeratotic poikiloderma
- Adult progeria
- AEC syndrome
- Albright's disease
- Alopecia congenita with keratosis palmoplantaris
- Alpha-N-acetylgalactosaminidase deficiency
- Anhidrotic ectodermal dysplasia
- ARC syndrome
- Atrophoderma reticulata symmetrica faciei
- Atrophoderma reticulatum
- Atrophodermia reticulata symmetrica faciei
- Atrophodermia ulerythematosa
- Austin disease
- Autosomal dominant ichthyosis
- Autosomal recessive chondrodysplasia punctata type 1
B
C
- CAP syndrome
- Cardio-facio-cutaneous syndrome
- Cardiocutaneous syndrome
- Chondrodystrophia calcificans punctata
- Chromatophore nevus of Naegeli
- Classic porokeratosis
- Clouston syndrome
- Cockayne syndrome complex
- Collodion baby
- Congenital absence of skin
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
- Congenital poikiloderma with blisters and keratoses
- Congenital poikiloderma with bullae and progressive cutaneous atrophy
- Congenital scars
- Continual peeling skin syndrome
- Cranio-carpo-tarsal syndrome
- Cutis aplasia
D
E
F
- Familial benign chronic pemphigus
- Familial colorectal polyposis
- Familial continual skin peeling
- Familial pancytopenia
- Familial panmyelophthisis
- Focal epidermolytic palmoplantar keratoderma
- Follicular atrophoderma and basal cell carcinomas
- Folliculitis rubra
- Folliculitis ulerythema reticulata
- Folliculitis ulerythematous reticulata
- Folliculitis ulerythemosa
G
H
- Happle syndrome
- Harlequin baby
- Harlequin fetus
- Harlequin ichthyosis
- Hereditary acrokeratotic poikiloderma
- Hereditary painful callosities
- Hereditary painful callosity syndrome
- Heredopathia atactica polyneuritiformis
- Herlitz disease
- Herlitz epidermolysis bullosa
- Herlitz syndrome
- Hidrotic ectodermal dysplasia
- Honeycomb atrophy
- HOPP syndrome
- Huriez syndrome
- Hypodontia with nail dysgenesis
- Hypomelanosis of Ito
I
K
L
M
N
P
- Palmoplantar ectodermal dysplasia type VIII
- Palmoplantar keratoderma and clubbing
- Palmoplantar keratoderma of the Norrbotten type
- Palmoplantar keratoderma with periodontitis
- Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis
- Palmoplantar keratoderma with scleroatrophy
- Palmoplantar keratoderma with sclerodactyly
- Papular atrichia
- Peroxisomal biogenesis disorder complementation group 11
- Phytanic acid storage disease
- Pityriasis circinata
- Plakophilin 1 deficiency
- Porokeratosis of Mibelli
- Progeria syndrome
- Progressive cardiomyopathic lentiginosis
- Progressive cribriform and zosteriform hyperpigmentation
R
S
- Scleroatrophic and keratotic dermatosis of the limbs
- Sclerotylosis
- Segmental neurofibromatosis
- Siemens-1 syndrome
- SNUB syndrome
- Steroid sulfatase deficiency
- Striate palmoplantar keratoderma with woolly hair and cardiomyopathy
- Striate palmoplantar keratoderma with woolly hair and left ventricular dilated cardiomyopathy
- Sulfur-deficient brittle hair syndrome