| 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 |
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 |
