|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence of one or more middle phalanx of a finger. (Human Phenotype Ontology, HP_0010239)|
|Downloads & Tools|
6 genes associated with the aplasia of the middle phalanx of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.