Rhabdomyolysis
Symptom Information:
| Symptom ID: | HPO:0003201 | ||||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle morphology(HPO:0011805) Rhabdomyolysis(HPO:0003201) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Myopathy(HPO:0003198) Rhabdomyolysis(HPO:0003201) |
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| Database Frequency: | 27 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
| Becker muscular dystrophy | (Orphanet:98895) |
| Carnitine palmitoyl transferase II deficiency | (Orphanet:157) |
| Carnitine palmitoyl transferase II deficiency, myopathic form | (Orphanet:228302) |
| Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
| Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency | (Orphanet:284426) |
| Glycogen storage disease due to lactate dehydrogenase deficiency | (Orphanet:2364) |
| Glycogen storage disease due to muscle glycogen phosphorylase deficiency | (Orphanet:368) |
| Glycogen storage disease due to phosphoglucomutase deficiency | (Orphanet:711) |
| Glycogen storage disease due to phosphoglycerate kinase 1 deficiency | (Orphanet:713) |
| Glycogen storage disease due to phosphoglycerate mutase deficiency | (Orphanet:97234) |
| Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
| Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
| King-Denborough syndrome | (Orphanet:99741) |
| Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
| MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4 | (OMIM:600467) |
| MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY | (OMIM:602199) |
| MELAS | (Orphanet:550) |
| Malignant hyperthermia | (Orphanet:423) |
| McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
| Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
| Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
| Myopathy due to myoadenylate deaminase deficiency | (OMIM:615511) |
| PGM1-CDG | (Orphanet:319646) |
| Thyrotoxic periodic paralysis | (Orphanet:79102) |
| Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
| Wilson disease | (Orphanet:905) |