|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes/proteins associated with the disease Marie Unna congenital hypotrichosis from the curated CTD Gene-Disease Associations dataset.