Category:Genodermatoses
From WikiMD.com Medical 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 200 pages are in this category, out of 299 total.
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- Acantholytic dyskeratotic epidermal nevus
- Acne vermoulanti
- Acral peeling skin syndrome
- Acrodermatitis
- Acrodermatitis enteropathica
- Acrogeria, Gottron type
- Acrokeratoelastoidosis of Costa
- 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
- ALOX12B
- 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
- Atrophoderma reticulata symmetrica faciei
- Atrophoderma reticulatum
- Atrophodermia reticulata symmetrica faciei
- Atrophodermia ulerythematosa
- Atrophodermie vermiculée des joues avec kératoses folliculaires
- Austin disease
- Autosomal dominant ichthyosis
- Autosomal recessive chondrodysplasia punctata type 1
B
- 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
- CAP syndrome
- Cardio-facio-cutaneous syndrome
- Cardiocutaneous syndrome
- Cardiofaciocutaneous syndrome
- CEDNIK syndrome
- Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
- CHILD syndrome
- Childhood tumor syndrome
- Chondrodysplasia punctata 1, X-linked recessive
- Chondrodystrophia calcificans punctata
- Chromatophore nevus of Naegeli
- Classic porokeratosis
- Clouston syndrome
- Clouston's hidrotic ectodermal dysplasia
- Cockayne syndrome
- Cockayne syndrome complex
- Collodion baby
- Colobomas of the eye–heart defects–ichthyosiform dermatosis–mental retardation–ear defects syndrome
- Congenital absence of skin
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
- Congenital poikiloderma with blisters and keratoses
- Congenital poikiloderma with bullae and progressive cutaneous atrophy
- Congenital scars
- Conradi–Hünermann–Happle syndrome
- Continual peeling skin syndrome
- Costello syndrome
- Cranio-carpo-tarsal syndrome
- Crouzon syndrome
- Crow–Fukase syndrome
- Cutis aplasia
D
- Darier–White disease
- Delleman–Oorthuys syndrome
- 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
- Distal arthrogryposis type 2
- Dorfman–Chanarin syndrome
- Dowling–Meara epidermolysis bullosa simplex
- Dyschromatosis universalis hereditaria
- Dyskeratosis follicularis
- Dystrophic epidermolysis bullosa
E
- EEC syndrome
- Epidermolysa bullosa simplex with muscular dystrophy
- Epidermolysis bullosa
- Epidermolysis bullosa letalis
- Epidermolysis bullosa simplex
- Epidermolysis bullosa simplex, Dowling-Meara type
- Epidermolysis bullosa simplex, generalized
- Epidermolysis bullosa simplex, localized
- Epidermolysis bullosa, lethal acantholytic
- Epiloia
- Erythrokeratodermia figurata variabilis
- Erythrokeratodermia progressiva Burns
- Erythrokeratodermia progressiva symmetrica
- Erythrokeratodermia variabilis et progressiva
- Erythrokeratolysis hiemalis
F
- Familial benign chronic pemphigus
- Familial colorectal polyposis
- Familial continual skin peeling
- Familial pancytopenia
- Familial panmyelophthisis
- Finlay–Marks syndrome
- Fischer–Jacobsen–Clouston syndrome
- Focal epidermolytic palmoplantar keratoderma
- Follicular atrophoderma and basal cell carcinomas
- Folliculitis rubra
- Folliculitis ulerythema reticulata
- Folliculitis ulerythematous reticulata
- Folliculitis ulerythemosa
G
H
- Hallopeau–Siemens disease
- Hallopeau–Siemens variant of epidermolysis bullosa
- Happle syndrome
- Harlequin baby
- Harlequin fetus
- Harlequin ichthyosis
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
- Hereditary acrokeratotic poikiloderma
- Hereditary painful callosities
- Hereditary painful callosity syndrome
- Heredopathia atactica polyneuritiformis
- Herlitz disease
- Herlitz epidermolysis bullosa
- Herlitz syndrome
- Heterochromia iridum
- Hidrotic ectodermal dysplasia
- Honeycomb atrophy
- HOPP syndrome
- Huriez syndrome
- Hutchinson–Gilford progeria syndrome
- Hutchinson–Gilford syndrome
- Hyperkeratosis–hyperpigmentation syndrome
- Hypodontia with nail dysgenesis
- Hypomelanosis of Ito
- Hypotrichosis–lymphedema–telangiectasia syndrome
I
- Ichthyosiform erythroderma with corneal involvement and deafness
- Ichthyosis
- Ichthyosis congenita
- Ichthyosis congenita gravior
- Ichthyosis exfoliativa
- Ichthyosis follicularis
- Ichthyosis hystrix
- Ichthyosis hystrix of Curth–Macklin
- Ichthyosis simplex
- Ichthyosis–brittle hair–impaired intelligence–decreased fertility–short stature syndrome
- Idiopathic deciduous skin
- Idiopathic hypertrophic osteoathorpathy
- Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndrome
J
K
L
- Laryngo–onycho–cutaneous syndrome
- Lentiginosis profusa syndrome
- Lethal junctional epidermolysis bullosa
- Lichen pilaire ou xerodermie pilaire symmetrique de la face
- Lichen pilare
- Linear and whorled nevoid hypermelanosis
- Linear Darier disease
- Linear epidermal nevus syndrome
- Linear nevoid hyperpigmentation
- Louis-Bar syndrome
- Louis–Bar syndrome
M
- Mandibulofacial dysostosis
- McCune–Albright syndrome
- McKusick type metaphyseal chondrodysplasia
- MELAS syndrome
- Mendes da Costa type erythrokeratodermia
- Microphthalmia with linear skin defects syndrome
- MIDAS syndrome
- Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes
- Moynahan syndrome
- Mucosulfatidosis
- Multiple lentigines syndrome
