| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A reduction of skin color related to a decrease in melanin production and deposition. (Human Phenotype Ontology, HP_0001010) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D017496 |
| Similar Terms | |
| Downloads & Tools |
2 genes/proteins associated with the disease Hypopigmentation from the curated CTD Gene-Disease Associations dataset.
