Hypertrichosis lanuginosa congenita

rare

Hypertrichosis lanuginosa congenita is a rare congenital skin disease characterized by the presence of 3 to 5cm long lanugo-type hair on the entire body, with the exception of palms, soles, and mucous membranes.

Identifiers: MONDO:0016381 OMIM:145700 Orphanet:2222
Part of: Ectodermal dysplasia syndrome Hypertrichosis
Also known as: congenital hypertrichosis lanuginosa · hypertrichosis lanuginosa universalis · hypertrichosis universalis

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Ambras type hypertrichosis universalis congenita	MONDO:0007787
X-linked congenital generalized hypertrichosis	MONDO:0010614

Rare disease

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