| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0010008 |
| Similar Terms | |
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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.
| Symbol | Name |
|---|---|
| RAB23 | RAB23, member RAS oncogene family |
