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Hypotrichosis 9

MONDO:0013649

A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 10q11.23-q22.3.

Also known as: HYPT9, hypotrichosis 9, hypotrichosis type 9, hypt9

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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