|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles. (Human Disease Ontology, DOID_4535)|
|Downloads & Tools|
3 genes/proteins associated with the disease Hypotrichosis from the curated CTD Gene-Disease Associations dataset.