Genodermatoses
Topic: Category
From HandWiki - Reading time: 4 min
Here is a list of articles in the category Genodermatoses of the Medicine portal.
 | 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.
Pages in category "Genodermatoses"
The following 200 pages are in this category, out of 309 total.
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- Medicine:Acantholytic dyskeratotic epidermal nevus
- Medicine:Acne vermoulanti
- Medicine:Acro–dermato–ungual–lacrimal–tooth syndrome
- Medicine:Acrocephalosyndactylia
- Medicine:Acrocephalosyndactyly
- Medicine:Acrodermatitis
- Medicine:Acrodermatitis enteropathica
- Medicine:Acrogeria
- Medicine:Acrokeratosis verruciformis
- Medicine:Acrokeratotic poikiloderma
- Medicine:Adams–Oliver syndrome
- Medicine:Albright's disease
- Medicine:Alopecia congenita with keratosis palmoplantaris
- Medicine:Angelman syndrome
- Medicine:Anhidrotic ectodermal dysplasia
- Medicine:Ankyloblepharon filiforme adnatum–ectodermal dysplasia–cleft palate syndrome
- Medicine:Ankyloblepharon–ectodermal defects–cleft lip and palate syndrome
- Medicine:Ankyloblepharon–ectodermal dysplasia–clefting syndrome
- Medicine:Arthrogryposis–renal dysfunction–cholestasis syndrome
- Medicine:Ataxia-telangiectasia
- Medicine:Atrichia with papular lesions
- Medicine:Atrophoderma reticulatum
- Medicine:Atrophodermia ulerythematosa
- Medicine:Atrophodermia vermiculata
- Medicine:Atrophodermie vermiculée des joues avec kératoses folliculaires
- Medicine:Austin disease
- Medicine:Autosomal dominant multiple pterygium syndrome
- Medicine:Autosomal recessive chondrodysplasia punctata type 1
B
- Medicine:Bart syndrome
- Medicine:Bazex syndrome
- Medicine:Bazex–Dupré–Christol syndrome
- Medicine:Beare–Stevenson cutis gyrata syndrome
- Medicine:Blau syndrome
- Medicine:Bloom syndrome
- Medicine:Bloom–Torre–Machacek syndrome
- Medicine:Bourneville disease
- Medicine:Brittle hair–intellectual impairment–decreased fertility–short stature syndrome
- Medicine:Bullous acrokeratotic poikiloderma of Kindler and Weary
- Medicine:Bullous congenital ichthyosiform erythroderma
- Medicine:Bullous ichthyosiform erythroderma
C
- Medicine:Cantú syndrome
- Medicine:Cardiocutaneous syndrome
- Medicine:Cardiofaciocutaneous syndrome
- Medicine:Cartilage–hair hypoplasia
- Medicine:CEDNIK syndrome
- Medicine:Childhood tumor syndrome
- Medicine:CHIME syndrome
- Medicine:Chondrodysplasia punctata
- Medicine:Chondrodystrophia calcificans punctata
- Medicine:Chromatophore nevus of Naegeli
- Medicine:Clouston syndrome
- Medicine:Clouston's hidrotic ectodermal dysplasia
- Medicine:Cockayne syndrome
- Medicine:Cockayne syndrome complex
- Medicine:Cockayne-Touraine disease
- Medicine:Collodion baby
- Medicine:Confluent and reticulated papillomatosis
- Medicine:Congenital absence of skin
- Medicine:Congenital ichthyosiform erythroderma
- Medicine:Congenital scars
- Medicine:Conradi–Hünermann syndrome
- Medicine:Conradi–Hünermann–Happle syndrome
- Medicine:Cortes Lacassie syndrome
- Medicine:Costello syndrome
- Medicine:Cronkhite–Canada syndrome
- Medicine:Crouzon syndrome
- Medicine:Cutis aplasia
D
- Medicine:Darier's disease
- Medicine:Delleman–Oorthuys syndrome
- Medicine:Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans
- Medicine:Dermatopathia pigmentosa reticularis hypohidotica et atrophica
- Medicine:DeSanctis–Cacchione syndrome
- Medicine:Desmons' syndrome
- Medicine:Distal arthrogryposis type 2
- Medicine:Dolichol kinase deficiency
- Medicine:Dorfman–Chanarin syndrome
- Medicine:Dowling–Meara epidermolysis bullosa simplex
- Medicine:Dyschromatosis universalis hereditaria
- Medicine:Dyskeratosis congenita
- Medicine:Dystrophic epidermolysis bullosa
E
- Medicine:Ectrodactyly–ectodermal dysplasia–cleft syndrome
- Medicine:EEC syndrome
- Medicine:Ellis–Van Creveld syndrome
- Medicine:Ellis–van Creveld syndrome
- Medicine:Epidermolysis bullosa dystrophica
- Medicine:Epidermolysis bullosa simplex
- Medicine:Epiloia
- Medicine:Erythrokeratodermia
- Medicine:Erythrokeratodermia figurata variabilis
- Medicine:Erythrokeratodermia progressiva Burns
- Medicine:Erythrokeratodermia progressiva symmetrica
- Medicine:Erythrokeratodermia variabilis
- Medicine:Erythrokeratodermia with ataxia
- Medicine:Erythrokeratolysis hiemalis
F
- Medicine:Familial benign chronic pemphigus
- Medicine:Familial colorectal polyposis
- Medicine:Fibrodysplasia ossificans progressiva
- Medicine:Finlay–Marks syndrome
- Medicine:Fischer–Jacobsen–Clouston syndrome
- Medicine:Focal dermal hypoplasia
- Medicine:Focal epidermolytic palmoplantar keratoderma
- Medicine:Follicular atrophoderma
- Medicine:Follicular atrophoderma and basal cell carcinomas
- Medicine:Folliculitis rubra
- Medicine:Folliculitis ulerythema reticulata
- Medicine:Folliculitis ulerythematous reticulata
- Medicine:Franceschetti–Klein syndrome
- Medicine:Freeman–Sheldon syndrome
G
H
- Medicine:Haber syndrome
- Medicine:Haim–Munk syndrome
- Medicine:Harlequin baby
- Medicine:Harlequin fetus
- Medicine:Harlequin-type ichthyosis
- Medicine:Hay–Wells syndrome
- Medicine:Hereditary acrokeratotic poikiloderma
- Medicine:Hereditary painful callosities
- Medicine:Hereditary painful callosity syndrome
- Medicine:Hereditary sclerosing poikiloderma
- Medicine:Heredopathia atactica polyneuritiformis
- Medicine:Herlitz disease
- Medicine:Herlitz epidermolysis bullosa
- Medicine:Herlitz syndrome
- Medicine:Heterochromia iridum
- Medicine:Hidrotic ectodermal dysplasia
- Medicine:Holocarboxylase synthetase deficiency
- Medicine:HOPP syndrome
- Medicine:Hutchinson–Gilford progeria syndrome
- Medicine:Hutchinson–Gilford syndrome
- Medicine:Hypohidrotic ectodermal dysplasia
- Medicine:Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
I
- Medicine:Ichthyosiform erythroderma with corneal involvement and deafness
- Medicine:Ichthyosiform erythroderma, corneal involvement, and deafness
- Medicine:Ichthyosis
- Medicine:Ichthyosis congenita
- Medicine:Ichthyosis exfoliativa
- Medicine:Ichthyosis follicularis
- Medicine:Ichthyosis follicularis, alopecia, and photophobia syndrome
- Medicine:Ichthyosis hystrix
- Medicine:Ichthyosis hystrix of Curth–Macklin
- Medicine:Ichthyosis linearis circumflexa
- Medicine:Ichthyosis prematurity syndrome
- Medicine:Ichthyosis vulgaris
- Medicine:Ichthyosis with confetti
- Medicine:Ichthyosis–brittle hair–impaired intelligence–decreased fertility–short stature syndrome
- Medicine:Idiopathic deciduous skin
- Medicine:Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndrome
- Medicine:Incontinentia pigmenti achromians
- Medicine:Infantile Refsum disease
J
K
- Medicine:Kabuki syndrome
- Medicine:Kanzaki disease
- Medicine:Keratitis–ichthyosis–deafness syndrome
- Medicine:Keratolysis exfoliativa congenita
- Medicine:Keratolytic winter erythema
- Medicine:Keratosis follicularis
- Medicine:Keratosis follicularis spinulosa decalvans
- Medicine:Keratosis palmaris with drumstick fingers
- Medicine:Keratosis pilaris atrophicans faciei
- Medicine:Keratosis pilaris rubra atrophicans faciei
- Medicine:KID syndrome
- Medicine:Kindler syndrome
- Medicine:KLICK syndrome
- Medicine:Klippel–Feil syndrome
L
- Medicine:Lamellar ichthyosis
- Medicine:Laryngo-onycho-cutaneous syndrome
- Medicine:Legius syndrome
- Medicine:Lelis syndrome
- Medicine:Lentiginosis
- Medicine:Lentiginosis profusa syndrome
- Medicine:Lenz–Majewski syndrome
- Medicine:Leschke syndrome
- Medicine:Lethal acantholytic epidermolysis bullosa
- Medicine:Lethal junctional epidermolysis bullosa
- Medicine:Lichen pilare
- Medicine:Linear nevoid hyperpigmentation
- Medicine:Louis–Bar syndrome
Licensed under CC BY-SA 3.0 | Source: https://handwiki.org/wiki/Category:Genodermatoses48 views | ↧ Download this article as ZWI file
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