Hypotrichosis 10

MONDO:0013650

A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 7p22.3-p21.3.

Also known as: HYPT10, hypotrichosis 10, hypotrichosis type 10, hypt10

0 clinical trials for this condition and its sub-types, 0 tagged with Hypotrichosis 10 itself.

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