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, 0 tagged with Hypotrichosis 9 itself.

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