Marie Unna hereditary hypotrichosis
MONDO:0018631A rare autosomal dominant hair loss disorder characterized by the absence or scarcity of scalp hair, eyebrows, and eyelashes at birth; coarse and wiry hair during childhood; and progressive hair loss beginning around puberty.
Also known as: HR hypotrichosis, MUHH, Marie Unna congenital hypotrichosis, hypotrichosis caused by mutation in HR, hypotrichosis, Marie Unna type
0 clinical trials for this condition and its sub-types, 0 tagged with Marie Unna hereditary hypotrichosis itself.
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Sub-types of Marie Unna hereditary hypotrichosis
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Hypotrichosis 4 0 trials
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Hypotrichosis 5 0 trials
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