proximal femoral metaphyseal irregularity Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Irregularity of the normally smooth surface of the proximal metaphysis of the femur. (Human Phenotype Ontology, HP_0003411)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003411
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Genes

1 genes associated with the proximal femoral metaphyseal irregularity 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