superior rectus atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophy of the superior rectus, the extraocular muscle whose primary function is to elevate the globe. (Human Phenotype Ontology, HP_0012242)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012242
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Genes

1 genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KIF21A kinesin family member 21A