Category:Genodermatoses
From WikiMD's Wellness Encyclopedia
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Genodermatoses are inherited genetic skin conditions often grouped into three categories—chromosomal, single gene, and polygenetic.
Pages in category "Genodermatoses"
The following 181 pages are in this category, out of 181 total.
A
- Acantholytic dyskeratotic epidermal nevus
- Acne vermoulanti
- Acrodermatitis
- Acrodermatitis enteropathica
- Acrogeria, Gottron type
- Acrokeratosis verruciformis of Hopf
- Adams–Oliver syndrome
- Adult progeria
- AEC syndrome
- Albright's hereditary osteodystrophy
- ALOX12B
- Angelman syndrome
- Ankyloblepharon filiforme adnatum–ectodermal dysplasia–cleft palate syndrome
- Ankyloblepharon–ectodermal defects–cleft lip and palate syndrome
- Ankyloblepharon–ectodermal dysplasia–clefting syndrome
- Apert syndrome
- Ataxia telangiectasia
- Atrophoderma reticulata symmetrica faciei
- Atrophoderma reticulatum
- Atrophodermia reticulata symmetrica faciei
- Atrophodermia ulerythematosa
- Atrophodermie vermiculée des joues avec kératoses folliculaires
B
C
- CAP syndrome
- Cardiofaciocutaneous syndrome
- CEDNIK syndrome
- Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
- CHILD syndrome
- Childhood tumor syndrome
- Chondrodysplasia punctata 1, X-linked recessive
- Clouston's hidrotic ectodermal dysplasia
- Cockayne syndrome
- Collodion baby
- Colobomas of the eye–heart defects–ichthyosiform dermatosis–mental retardation–ear defects syndrome
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
- Nonbullous congenital ichthyosiform erythroderma
- Congenital poikiloderma with blisters and keratoses
- Congenital poikiloderma with bullae and progressive cutaneous atrophy
- Costello syndrome
- Crouzon syndrome
D
- Darier disease
- Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans
- Dermatopathia pigmentosa reticularis hypohidotica et atrophica
- Desmons' syndrome
- Diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy
- Disseminated superficial actinic porokeratosis
- Dominant dystrophic epidermolysis bullosa
- Dyschromatosis universalis hereditaria
- Dystrophic epidermolysis bullosa
E
- Epidermolysa bullosa simplex with muscular dystrophy
- Epidermolysis bullosa
- Epidermolysis bullosa simplex
- Epidermolysis bullosa simplex, Dowling-Meara type
- Epidermolysis bullosa simplex, generalized
- Epidermolysis bullosa simplex, localized
- Epidermolysis bullosa, lethal acantholytic
- Erythrokeratodermia progressiva symmetrica
- Erythrokeratodermia variabilis et progressiva
F
G
H
- Hallopeau–Siemens variant of epidermolysis bullosa
- Happle syndrome
- Harlequin ichthyosis
- Harlequin-type ichthyosis
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
- Heterochromia iridum
- Honeycomb atrophy
- HOPP syndrome
- Hypodontia with nail dysgenesis
- Hypomelanosis of Ito
- Hypotrichosis–lymphedema–telangiectasia syndrome
I
- Ichthyosiform erythroderma with corneal involvement and deafness
- Ichthyosis
- Ichthyosis hystrix
- Ichthyosis hystrix, Curth Macklin type
- Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
- Ichthyosis–brittle hair–impaired intelligence–decreased fertility–short stature syndrome
- Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndrome
- Infantile Refsum disease
K
L
M
N
P
- Palmoplantar keratoderma of the Norrbotten type
- Palmoplantar keratoderma with periodontitis
- Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis
- Papillon Lefevre syndrome
- Papular atrichia
- Peroxisomal biogenesis disorder complementation group 11
- Photosensitivity–ichthyosis–brittle sulfur-deficient hair–impaired intelligence–decreased fertility–short stature syndrome
- Pityriasis circinata
- Plakophilin 1 deficiency
- POEMS syndrome
- Polyneuropathy–organomegaly–endocrinopathy–monoclonal gammopathy–skin changes syndrome
- Popliteal pterygium syndrome
- Pretibial epidermolysis bullosa
- Progeria
- Progressive cribriform and zosteriform hyperpigmentation
- Progressive osseous heteroplasia
- Proteus syndrome
- Proteus-like syndrome
R
S
- Schindler disease
- Schindler disease type 1
- Scleroatrophic and keratotic dermatosis of the limbs
- Segmental neurofibromatosis
- Severe generalized recessive dystrophic epidermolysis bullosa
- Sjögren–Larsson syndrome
- SNUB syndrome
- Split hand–split foot–ectodermal dysplasia–cleft syndrome
- Striate palmoplantar keratoderma with woolly hair and cardiomyopathy
- Striate palmoplantar keratoderma with woolly hair and left ventricular dilated cardiomyopathy
- Sturge-Weber syndrome
