|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of the pigmentation of the mucosa of the mouth. (Human Phenotype Ontology, HP_0100669)|
|Downloads & Tools|
4 genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.