proximal radio-ulnar synostosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal osseous union (fusion) between the proximal portions of the radius and the ulna. (Human Phenotype Ontology, HP_0005037)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005037
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Genes

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.

Symbol Name
HOXA11 homeobox A11