Hypotrichosis 8

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.