Phenotypic Feature Rhabdomyolysis finds 8 Gene-Feature associations that are associated with 8 Genes
| Gene | OMIM Disease | Phenotypic Feature | Phenotype Annotation | Clinical Category | PMIDs |
|---|---|---|---|---|---|
| ACADM | 201450 | Rhabdomyolysis | acute muscle necrosis | musculoskeletal | 7876853 11524729 |
| ACADVL | 201475 | Rhabdomyolysis | painful; attacks; dark urine | musculoskeletal | 9546340 10910451 16443431 |
| CPT1A | 255120 | Rhabdomyolysis | occasional | musculoskeletal | 11286380 11350183 |
| CPT2 | 255110 | Rhabdomyolysis | dark urine; recurrent episodes | musculoskeletal | 2748260 8358442 8786066 8815169 11999976 15642848 15776096 |
| DLD | 248600 | Rhabdomyolysis | marked rhabdomyolysis; episode | musculoskeletal | 9934985 |
| ETFA | 231680 | Rhabdomyolysis | acute rhabdomyolysis | musculoskeletal | 16510302 |
| HADHA | 609015 | Rhabdomyolysis | episodic | musculoskeletal | 15902556 |
| HADHB | 609015 | Rhabdomyolysis | episodes | musculoskeletal | 15617873 15902556 |
