| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An autosomal dominant disease that is characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive deafness. (Human Disease Ontology, DOID_0050788) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0100264 |
| Similar Terms | |
| Downloads & Tools |
2 genes associated with the proximal symphalangism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
