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.

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Broader categories

Disease (618) Hereditary disease (172) Alopecia (109) Human disease (14) Disorder of pilosebaceous unit (7) Hypotrichosis (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Hair anomaly (0)

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