| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D007039 |
| Similar Terms | |
| Downloads & Tools |
3 genes/proteins associated with the disease Hypotrichosis from the curated CTD Gene-Disease Associations dataset.
