|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||This term applies if one or more of the middle phalanges of the hand are either partially duplicated, depending on severity leading to a broad or bifid appearance of the phalanges, or completely duplicated. (Human Phenotype Ontology, HP_0010008)|
|Downloads & Tools|
1 genes associated with the duplication of the middle phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|RAB23||RAB23, member RAS oncogene family|