|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||This term applies if one or more of the phalanges of the 2nd finger are either partially duplicated, depending on severity leading to a broad or bifid appearance of the phalanges, or completely duplicated. (Human Phenotype Ontology, HP_0009945)|
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2 genes associated with the duplication of phalanx of 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.