general/genodermatoses
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Microphthalmia–dermal aplasia–sclerocornea syndrome (1)
Gingival fibromatosis with hypertrichosis (1)
Kindler syndrome (1)
Progressive symmetric erythrokeratodermia (1)
Erythrokeratodermia with ataxia (1)
Epidermolysis bullosa dystrophica (1)
Costello syndrome (1)
Haim–Munk syndrome (1)
Epidermolysis bullosa simplex (1)
Ichthyosis follicularis with alopecia and photophobia syndrome (1)
Skin fragility syndrome (1)
Ichthyosis bullosa of Siemens (1)
Bazex–Dupré–Christol syndrome (1)
Johnson–McMillin syndrome (1)
Porokeratosis (1)
Oculocerebrocutaneous syndrome (1)
XXYY syndrome (1)
Progressive osseous heteroplasia (1)
Genodermatosis (1)
Epidermolysis bullosa dystrophica (1)
Costello syndrome (1)
Haim–Munk syndrome (1)
Werner syndrome (1)
X-linked recessive chondrodysplasia punctata (1)
Lethal acantholytic epidermolysis bullosa (1)
Crouzon syndrome (1)
Junctional epidermolysis bullosa (medicine) (1)
Werner syndrome (1)
X-linked recessive chondrodysplasia punctata (1)
Pachyonychia congenita (1)
Naegeli–Franceschetti–Jadassohn syndrome (1)
McCune–Albright syndrome (1)
Werner syndrome (1)
X-linked recessive chondrodysplasia punctata (1)
Ichthyosis vulgaris (1)
Supernumerary nipples–uropathies–Becker's nevus syndrome (1)
Ichthyosis vulgaris (1)
Junctional epidermolysis bullosa (medicine) (1)
Legius syndrome (1)
Bart syndrome (1)
Supernumerary nipples–uropathies–Becker's nevus syndrome (1)
Marinesco–Sjögren syndrome (1)
Microphthalmia–dermal aplasia–sclerocornea syndrome (1)
Beare–Stevenson cutis gyrata syndrome (1)
Porokeratosis (1)
Disseminated superficial actinic porokeratosis (1)
Leschke syndrome (1)
Microphthalmia–dermal aplasia–sclerocornea syndrome (1)
Gingival fibromatosis with hypertrichosis (1)
Kindler syndrome (1)
Progressive symmetric erythrokeratodermia
Rare, genetic skin condition
Epidermolysis bullosa dystrophica
Medical condition
Oculocerebrocutaneous syndrome
Syndrome characterised by eye, central nervous system and skin malformations
XXYY syndrome
Extra X and Y chromosome in males
Progressive osseous heteroplasia
Rare genetic condition characterised by cutaneous or subcutaneous ossification
Genodermatosis
Genetic skin disease
Epidermolysis bullosa dystrophica
Medical condition
Crouzon syndrome
Genetic disorder of the skull and face
Junctional epidermolysis bullosa (medicine)
Medical condition
McCune–Albright syndrome
Mosaic genetic disorder affecting the bone, skin and endocrine systems
Ichthyosis vulgaris
Skin disorder
Ichthyosis vulgaris
Skin disorder
Junctional epidermolysis bullosa (medicine)
Medical condition
Beare–Stevenson cutis gyrata syndrome
Autosomal dominant genetic disorder
Leschke syndrome
Medical condition