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.
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Subcategories
This category has the following 3 subcategories, out of 3 total.
E
- Epidermolysis bullosa (11 P)
Σ
- Genodermatoses stubs (87 P)
Pages in category "Genodermatoses"
The following 200 pages are in this category, out of approximately 412 total. This list may not reflect recent changes.
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A
- Acantholytic dyskeratotic epidermal nevus
- Acne vermoulanti
- Acral peeling skin syndrome
- Acro–dermato–ungual–lacrimal–tooth syndrome
- Acrocephalosyndactyly
- Acrodermatitis
- Acrodermatitis enteropathica
- Acrogeria
- Acrokeratosis verruciformis
- Acrokeratosis verruciformis of Hopf
- Acrokeratotic poikiloderma
- Adams–Oliver syndrome
- Adult progeria
- AEC syndrome
- Albright's disease
- Albright's hereditary osteodystrophy
- Alopecia congenita with keratosis palmoplantaris
- Alpha-N-acetylgalactosaminidase deficiency
- Angelman syndrome
- Anhidrotic ectodermal dysplasia
- Ankyloblepharon filiforme adnatum–ectodermal dysplasia–cleft palate syndrome
- Ankyloblepharon–ectodermal defects–cleft lip and palate syndrome
- Ankyloblepharon–ectodermal dysplasia–clefting syndrome
- Apert syndrome
- ARC syndrome
- Arthrogryposis–renal dysfunction–cholestasis syndrome
- Ataxia–telangiectasia
- Atrichia with papular lesions
- Atrophoderma reticulata symmetrica faciei
- Atrophoderma reticulatum
- Atrophodermia reticulata symmetrica faciei
- Atrophodermia ulerythematosa
- Atrophodermia vermiculata
- Atrophodermie vermiculée des joues avec kératoses folliculaires
- Austin disease
- Autosomal dominant ichthyosis
- Autosomal dominant multiple pterygium syndrome
- Autosomal recessive chondrodysplasia punctata type 1
B
- Bart syndrome
- Bazex syndrome
- Bazex–Dupré–Christol syndrome
- Beare–Stevenson cutis gyrata syndrome
- Blau syndrome
- Bloom syndrome
- Bloom–Torre–Machacek syndrome
- Blue rubber bleb nevus syndrome
- Bourneville disease
- Brittle hair–intellectual impairment–decreased fertility–short stature syndrome
- Bullous acrokeratotic poikiloderma of Kindler and Weary
- Bullous congenital ichthyosiform erythroderma
- Bullous ichthyosiform erythroderma
C
- Cantú syndrome
- CAP syndrome
- Cardio-facio-cutaneous syndrome
- Cardiocutaneous syndrome
- Cardiofaciocutaneous syndrome
- Cartilage–hair hypoplasia
- CEDNIK syndrome
- CHILD syndrome
- Childhood tumor syndrome
- CHIME syndrome
- Chondrodysplasia punctata
- Chondrodystrophia calcificans punctata
- Chromatophore nevus of Naegeli
- Classic porokeratosis
- Clouston syndrome
- Clouston's hidrotic ectodermal dysplasia
- Cockayne syndrome
- Cockayne syndrome complex
- Cockayne-Touraine disease
- Collodion baby
- Colobomas of the eye–heart defects–ichthyosiform dermatosis–mental retardation–ear defects syndrome
- Confluent and reticulated papillomatosis
- Congenital absence of skin
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
- Congenital ichthyosiform erythroderma
- Congenital poikiloderma with blisters and keratoses
- Congenital poikiloderma with bullae and progressive cutaneous atrophy
- Congenital scars
- Conradi–Hünermann syndrome
- Conradi–Hünermann–Happle syndrome
- Continual peeling skin syndrome
- Cortes Lacassie syndrome
- Costello syndrome
- Cranio-carpo-tarsal syndrome
- Craniosynostosis–anal anomalies–porokeratosis syndrome
- Cronkhite–Canada syndrome
- Crouzon syndrome
- Crow–Fukase syndrome
- Cutis aplasia
- Cutis verticis gyrata
D
- Darier–White disease
- Darier's disease
- Delleman–Oorthuys syndrome
- Dermatopathia pigmentosa reticularis
- Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans
- Dermatopathia pigmentosa reticularis hypohidotica et atrophica
- DeSanctis–Cacchione syndrome
- Desmons' syndrome
- Diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy
- Disseminated superficial actinic porokeratosis
- Distal arthrogryposis type 2
- Dolichol kinase deficiency
- Dorfman–Chanarin syndrome
- Dowling–Meara epidermolysis bullosa simplex
- Dyschromatosis universalis hereditaria
- Dyskeratosis congenita
- Dyskeratosis follicularis
E
- Ectodermal dysplasia
- Ectodermal dysplasia with corkscrew hairs
- Ectrodactyly–ectodermal dysplasia–cleft syndrome
- EEC syndrome
- Ehlers–Danlos syndrome
- Ellis–Van Creveld syndrome
- Epidermolysis bullosa letalis
- Epidermolytic hyperkeratosis
- Epiloia
- Erythrokeratodermia
- Erythrokeratodermia figurata variabilis
- Erythrokeratodermia progressiva Burns
- Erythrokeratodermia progressiva symmetrica
- Erythrokeratodermia variabilis
- Erythrokeratodermia with ataxia
- Erythrokeratolysis hiemalis
F
- Familial benign chronic pemphigus
- Familial colorectal polyposis
- Familial continual skin peeling
- Familial pancytopenia
- Familial panmyelophthisis
- Fibrodysplasia ossificans progressiva
- Finlay–Marks syndrome
- Fischer–Jacobsen–Clouston syndrome
- Focal dermal hypoplasia
- Focal epidermolytic palmoplantar keratoderma
- Follicular atrophoderma
- Follicular atrophoderma and basal cell carcinomas
- Folliculitis rubra
- Folliculitis ulerythema reticulata
- Folliculitis ulerythematous reticulata
- Folliculitis ulerythemosa
- Freeman–Sheldon syndrome
G
H
- Haber syndrome
- Hailey–Hailey disease
- Haim–Munk syndrome
- Hallopeau–Siemens disease
- Hallopeau–Siemens variant of epidermolysis bullosa
- Happle syndrome
- Harlequin baby
- Harlequin fetus
- Harlequin ichthyosis
- Harlequin-type ichthyosis
- Hay–Wells syndrome
- Hereditary acrokeratotic poikiloderma
- Hereditary painful callosities
- Hereditary painful callosity syndrome
- Hereditary sclerosing poikiloderma
- Heredopathia atactica polyneuritiformis
- Herlitz disease
- Herlitz epidermolysis bullosa
- Herlitz syndrome
- Heterochromia
- Hidrotic ectodermal dysplasia
- Holocarboxylase synthetase deficiency
- Honeycomb atrophy
- HOPP syndrome
- Huriez syndrome
- Hutchinson–Gilford progeria syndrome
- Hutchinson–Gilford syndrome
- Hyperkeratosis–hyperpigmentation syndrome
- Hypodontia with nail dysgenesis
- Hypohidrotic ectodermal dysplasia
- Hypomelanosis of Ito
- Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
- Hypotrichosis–lymphedema–telangiectasia syndrome
I
- Ichthyosiform erythroderma with corneal involvement and deafness
- Ichthyosiform erythroderma, corneal involvement, and deafness
- Ichthyosis
- Ichthyosis bullosa of Siemens
- Ichthyosis congenita
- Ichthyosis congenita gravior
- Ichthyosis exfoliativa
- Ichthyosis follicularis
- Ichthyosis follicularis with alopecia and photophobia syndrome
- Ichthyosis follicularis, alopecia, and photophobia syndrome
- Ichthyosis hystrix
- Ichthyosis hystrix of Curth–Macklin
- Ichthyosis linearis circumflexa
- Ichthyosis prematurity syndrome