abnormality of upper limb metaphysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of one or more metaphyses of the arms. (Human Phenotype Ontology, HP_0009809)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009809
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Genes

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.

Symbol Name
TRPV4 transient receptor potential cation channel, subfamily V, member 4