hypotrichosis 7 (MONDO_0011452) can be described as follows. 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 caused by mutation in LIPH, hypotrichosis type 7, hypotrichosis, localized, autosomal recessive 2, total Mari type hypotrichosis,.