Hypotrichosis 2

MONDO:0007805

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

Also known as: CDSN hypotrichosis, HYPT2, hypotrichosis 2, hypotrichosis caused by mutation in CDSN, hypotrichosis simplex of the scalp 1, hypotrichosis type 2, hypt2, Htss

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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