|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence of the middle phalanx of the little (5th) finger. (Human Phenotype Ontology, HP_0009162)|
|Downloads & Tools|
1 genes associated with the absent middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|GJA1||gap junction protein, alpha 1, 43kDa|