Hypotrichosis 7

MONDO:0011452

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

Also known as: HYPT7, LAH2, LIPH hypotrichosis, Lah2, hypotrichosis 7, hypotrichosis caused by mutation in LIPH, hypotrichosis type 7, hypotrichosis, localized, autosomal recessive 2

0 clinical trials for this condition and its sub-types, 0 tagged with Hypotrichosis 7 itself.

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↑ Hypotrichosis (6) ↑ Hypotrichosis simplex (0) ↑ Isolated familial wooly hair disorder (0)

Including sub-types (0) Tagged with Hypotrichosis 7 (0)

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