Hypotrichosis 8

MONDO:0010206

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

Also known as: HYPT8, LAH3, LPAR6 hypotrichosis, hypotrichosis 8, hypotrichosis caused by mutation in LPAR6, hypotrichosis type 8, hypotrichosis, localized, autosomal recessive 3, woolly hair, autosomal recessive 1, with or without hypotrichosis

0 clinical trials for this condition and its sub-types, 0 tagged with Hypotrichosis 8 itself.

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

Including sub-types (0) Tagged with Hypotrichosis 8 (0)

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