Marie Unna congenital hypotrichosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Marie Unna hereditary hypotrichosis (MUHH) is a 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. (Orphanet Rare Disease Ontology, Orphanet_444)
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2 genes/proteins associated with the disease Marie Unna congenital hypotrichosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HMU Hypotrichosis, Marie Unna type 2.88009
HR hair growth associated 2.88009