Hypotrichosis 1

MONDO:0011549

Any hypotrichosis in which the cause of the disease is a mutation in the APCDD1 gene.

Also known as: HHS, APCDD1 hypotrichosis, HTS, HYPT1, hereditary generalised hypotrichosis simplex, hypotrichosis 1, hypotrichosis caused by mutation in APCDD1, hypotrichosis type 1

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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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