|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An anomaly of one or more metaphyses of the arms. (Human Phenotype Ontology, HP_0009809)|
|Downloads & Tools|
1 genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|TRPV4||transient receptor potential cation channel, subfamily V, member 4|