Category:Genodermatoses
From WikiMD.com - Food, Medicine & Wellness Encyclopedia
Genodermatoses are inherited genetic skin conditions often grouped into three categories—chromosomal, single gene, and polygenetic.
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Pages in category "Genodermatoses"
The following 200 pages are in this category, out of 289 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
- Adult progeria
- AEC syndrome
- Albright's disease
- 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
- 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
- Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma 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
- 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
- Distal arthrogryposis type 2
- Dorfman–Chanarin syndrome
- Dowling–Meara epidermolysis bullosa simplex
- 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 disseminated comedones without dyskeratosis
- 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
- Multiple sulfatase deficiency
- Mutilating palmoplantar keratoderma of the Gamborg–Nielsen type
