Acute rhabdomyolysis

Symptom Information:

Symptom ID: HPO:0008942
Synonyms:
Rhabdomyolysis, acute [HPO:0008942]
Rhabdomyolysis, acute [OMIM:Rhabdomyolysis, acute]
Quality:
Cross references:
OMIM: "Rhabdomyolysis, acute" [OMIM:Rhabdomyolysis, acute]
Is a (Direct Parents):
HPO         Rhabdomyolysis
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)
                Acute rhabdomyolysis(HPO:0008942)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Genetic recurrent myoglobinuria (Orphanet:99845)