| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Hypoplasia (congenital reduction in size) of the middle phalanx of the second finger, also known as the index finger. (Human Phenotype Ontology, HP_0009577) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009577 |
| Similar Terms | |
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1 genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| RUNX2 | runt-related transcription factor 2 |
