Any hypotrichosis in which the cause of the disease is a mutation in the LPAR6 gene. The disease is hypotrichosis 8 (MONDO_0010206). Also known as: HYPT8, LAH3, LPAR6 hypotrichosis, hypotrichosis caused by mutation in LPAR6, hypotrichosis type 8, hypotrichosis, localized, autosomal recessive 3.