| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Lack of skin pigmentation (coloring) of the chest. (Human Phenotype Ontology, HP_0040007) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0040007 |
| Similar Terms | |
| Downloads & Tools |
2 genes associated with the absent pigmentation of chest phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
