Category:Genodermatoses
Jump to navigation
Jump to search
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.
Pages in category "Genodermatoses"
The following 144 pages are in this category, out of 144 total.
A
- Acantholytic dyskeratotic epidermal nevus
- Acro–dermato–ungual–lacrimal–tooth syndrome
- Acrocephalosyndactyly
- Acrodermatitis
- Acrodermatitis enteropathica
- 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
- Cardiofaciocutaneous syndrome
- Cartilage–hair hypoplasia
- CEDNIK syndrome
- CHILD syndrome
- CHIME syndrome
- Chondrodysplasia punctata
- Clouston's hidrotic ectodermal dysplasia
- Cockayne syndrome
- Confluent and reticulated papillomatosis
- Congenital ichthyosiform erythroderma
- Conradi–Hünermann syndrome
- Costello syndrome
- Cronkhite–Canada syndrome
- Crouzon syndrome
- Cutis verticis gyrata
D
E
F
H
I
J
K
L
M
N
O
P
- Pachydermoperiostosis
- Pachyonychia congenita
- Papillon–Lefèvre syndrome
- Pityriasis rotunda
- POEMS syndrome
- Polyostotic fibrous dysplasia
- Popliteal pterygium syndrome
- Porokeratosis
- Prader–Willi syndrome
- Progeria
- Progressive osseous heteroplasia
- Progressive symmetric erythrokeratodermia
- Proteus syndrome