|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormal osseous union (fusion) between the proximal portions of the radius and the ulna. (Human Phenotype Ontology, HP_0005037)|
|Downloads & Tools|
1 genes associated with the proximal radio-ulnar synostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.