Category:Genodermatoses
Pages in this category should be moved to subcategories where applicable. This category may require frequent maintenance to avoid becoming too large. It should directly contain very few, if any, pages and should mainly contain subcategories.
Genodermatoses are inherited genetic skin conditions often grouped into three categories—chromosomal, single gene, and polygenetic.
Wikimedia Commons has media related to Genodermatoses.
Subcategories
This category has the following 3 subcategories, out of 3 total.
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Pages in category "Genodermatoses"
The following 191 pages are in this category, out of 191 total.
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A
- Acantholytic dyskeratotic epidermal nevus
- ADULT syndrome
- Acrocephalosyndactyly
- Acrodermatitis
- Acrodermatitis enteropathica
- Acrogeria
- Acrokeratosis verruciformis
- Adams–Oliver syndrome
- Albright's hereditary osteodystrophy
- Angelman syndrome
- Apert syndrome
- Arthrogryposis–renal dysfunction–cholestasis syndrome
- Ataxia–telangiectasia
- Atrichia with papular lesions
- Atrophodermia vermiculata
- Autosomal dominant multiple pterygium syndrome
B
C
- Cantú syndrome
- Cardiofaciocutaneous syndrome
- Cartilage–hair hypoplasia
- CEDNIK syndrome
- CHILD syndrome
- Childhood tumor syndrome
- CHIME syndrome
- Chondrodysplasia punctata
- Clouston's hidrotic ectodermal dysplasia
- Cockayne syndrome
- Confluent and reticulated papillomatosis
- Congenital ichthyosiform erythroderma
- Conradi–Hünermann syndrome
- Cortes Lacassie syndrome
- Costello syndrome
- Craniosynostosis–anal anomalies–porokeratosis syndrome
- Cronkhite–Canada syndrome
- Crouzon syndrome
- Cutis verticis gyrata
D
E
F
G
H
- Haber syndrome
- Hailey–Hailey disease
- Haim–Munk syndrome
- Harlequin-type ichthyosis
- Hay–Wells syndrome
- Hereditary sclerosing poikiloderma
- Heterochromia
- Holocarboxylase synthetase deficiency
- Hypohidrotic ectodermal dysplasia
- Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
- Hypotrichosis–lymphedema–telangiectasia syndrome
I
K
L
M
N
O
P
- Pachyderma
- Pachydermoperiostosis
- Pachyonychia congenita
- Papillon–Lefèvre syndrome
- Peeling skin syndrome
- Pityriasis rotunda
- Plate-like osteoma cutis
- POEMS syndrome
- Polyostotic fibrous dysplasia
- Popliteal pterygium syndrome
- Porokeratosis
- Prader–Willi syndrome
- Progeria
- Progressive osseous heteroplasia
- Progressive symmetric erythrokeratodermia
- Proteus syndrome
- Proteus-like syndrome
R
S
T
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