acute rhabdomyolysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An acute form of rhabdomyolysis. (Human Phenotype Ontology, HP_0008942)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008942
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1