genetic disease of the skin (genodermatosis)
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More general terms
More specific terms
- acrodermatitis enteropathica
- actinic prurigo; hydroa estivale; Hutchinson's summer prurigo
- angiokeratoma of Mibelli
- anonychia congenita
- aplasia cutis
- atrichia with papular lesions
- benign familial pemphigus (Hailey-Hailey disease)
- Birt-Hogg-Dube syndrome
- cutis laxa; elastolysis; loose skin; pachydermatocele
- Darier-White disease; keratosis follicularis
- Dowling-Degos-Kitamura disease; Dowling-Degos disease; reticulate acropigmentation of Kitamura
- dyschromatosis symmetrical hereditaria (reticulate acropigmentation of Dohi)
- dyschromatosis universalis hereditaria
- dysplastic (Clark's) melanocytic nevus
- ectodermal dysplasia
- epidermal nevus epidermolytic hyperkeratotic type
- epidermodysplasia verruciformis
- epidermolysis bullosa acquisita (EBA)
- epidermolysis bullosa dystrophica (EBD)
- epidermolysis bullosa simplex (EBS)
- epidermolysis bullosa with pyloric atresia; aplasia cutis congenita with gastrointestinal atresia
- epidermolysis bullosa, junctional
- familial lichen planus
- familial progressive hyperpigmentation (melanosis universalis hereditaria)
- hypomelanosis of Ito (incontinentia pigmenti achromians)
- ichthyosis; erythrokeratodermia variabilis
- incontinentia pigmenti; Bloch-Sulzberger syndrome; familial incontinentia pigmenti type II
- knuckle pad
- Meleda disease; mal de meleda; keratosis palmoplantaris transgradiens
- Naegeli-Franceschetti-Jadassohn syndrome (NFJS); Naegeli syndrome
- Netherton syndrome; trichorrhexis invaginata; bamboo hair
- oculocutaneous albinism
- Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia type 1)
- Osler-Weber-Rendu syndrome 2; hereditary hemorrhagic telangiectasia type 2 (HHT2, ORW2)
- pachyonychia congenita
- palmoplantar keratoderma epidermolytic (EPPK, EHPPK)
- palmoplantar keratoderma striate
- peeling skin syndrome (keratosis exfoliativa congenita)
- piebaldism (partial albinism)
- primary localized cutaneous amyloidosis; familial lichen amyloidosis
- pseudoxanthoma elasticum (Gronold-Strandberg syndrome)
- PXE-like disorder with multiple coagulation factor deficiency; pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency
- skin fragility-woolly hair syndrome (SFWHS)
- steatocystoma multiplex
- unilateral palmoplantar verrucous nevus
- wrinkly skin syndrome
- xeroderma pigmentosum