Hypotrichosis 13

MONDO:0014390

Any hypotrichosis in which the cause of the disease is a mutation in the KRT71 gene.

Also known as: HYPT13, KRT71 hypotrichosis, hypotrichosis 13, hypotrichosis caused by mutation in KRT71, hypotrichosis type 13, hypotrichosis with woolly hair, hypotrichosis with wooly hair, hypt13

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) 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) Integumentary system disorder (0)

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