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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535912
Similar Terms
Downloads & Tools

Genes

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