|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Missing radius bone on both sides associated with congenital failure of development. (Human Phenotype Ontology, HP_0004977)|
|Downloads & Tools|
1 genes associated with the bilateral radial aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|RBM8A||RNA binding motif protein 8A|