Category:Genodermatoses
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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 2 subcategories, out of 2 total.
Σ
- Genodermatoses stubs (85 P)
Pages in category "Genodermatoses"
The following 200 pages are in this category, out of approximately 418 total. This list may not reflect recent changes.
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- 4p- syndrome
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
- Dystrophic epidermolysis bullosa
E
- Ectodermal dysplasia
- Ectodermal dysplasia with corkscrew hairs
- Ectrodactyly–ectodermal dysplasia–cleft syndrome
- EEC syndrome
- Ellis–Van Creveld syndrome
- Epidermolysis bullosa
- Epidermolysis bullosa dystrophica
- Epidermolysis bullosa letalis
- Epidermolysis bullosa simplex
- 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
- Franceschetti–Klein syndrome
- Freeman–Sheldon syndrome
G
- Gardner's syndrome
- Gastrocutaneous syndrome
- Generalized trichoepithelioma
- Genodermatosis
- Giant axonal neuropathy with curly hair
- Gingival fibromatosis with hypertrichosis
- Giroux–Barbeau syndrome
- Goltz syndrome
- Gorlin syndrome
- Gorlin syndrome II
- Gottron syndrome
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 iridum
- 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