Hypotrichosis 6

MONDO:0011932

Any hypotrichosis in which the cause of the disease is a mutation in the DSG4 gene.

Also known as: DSG4 hypotrichosis, HYPT6, LAH1, Lah1, autosomal recessive localised hypotrichosis, hypotrichosis 6, hypotrichosis caused by mutation in DSG4, hypotrichosis type 6

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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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