autosomal dominant palmoplantar keratoderma and congenital alopecia
Autosomal dominant palmoplantar keratoderma with congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications
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autosomal dominant palmoplantar keratoderma and congenital alopecia
Summary
autosomal dominant palmoplantar keratoderma and congenital alopecia is a developmental defect during embryogenesis[1].
Key Facts
- autosomal dominant palmoplantar keratoderma and congenital alopecia's instance of is recorded as developmental defect during embryogenesis[2].
- autosomal dominant palmoplantar keratoderma and congenital alopecia's instance of is recorded as rare disease[3].
- autosomal dominant palmoplantar keratoderma and congenital alopecia's instance of is recorded as class of disease[4].
- autosomal dominant palmoplantar keratoderma and congenital alopecia is a type of autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature[5].
- autosomal dominant palmoplantar keratoderma and congenital alopecia is a type of ectodermal dysplasia[6].
- autosomal dominant palmoplantar keratoderma and congenital alopecia's genetic association is recorded as GJA1[7].
- autosomal dominant palmoplantar keratoderma and congenital alopecia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1010[8].
- autosomal dominant palmoplantar keratoderma and congenital alopecia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111244[9].
- autosomal dominant palmoplantar keratoderma and congenital alopecia's exact match is recorded as http://identifiers.org/doid/DOID:0111244[10].
- autosomal dominant palmoplantar keratoderma and congenital alopecia's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].