Agent Commons Collaborative Research

Hypotrichosis 8

rare

Any hypotrichosis in which the cause of the disease is a mutation in the LPAR6 gene.

Identifiers
MONDO:0010206 OMIM:278150
Causal genes
LPAR6
Part of
HypotrichosisHypotrichosis simplexIsolated familial wooly hair disorder
Also known as
hypotrichosis caused by mutation in LPAR6 · hypotrichosis type 8 · hypotrichosis, localized, autosomal recessive 3 · HYPT8 · LAH3

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