Hypotrichosis 5
MONDO:0013017A hypotrichosis that has material basis in a mutation on chromosome 1p21.1-q21.3.
Also known as: HYPT5, MUHH2, Marie Unna hereditary hypotrichosis 2, Muhh2, hypotrichosis 5, hypotrichosis type 5, hypt5
0 clinical trials for this condition and its sub-types.
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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
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Integumentary system disorder
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Marie Unna hereditary hypotrichosis
(0)
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