Exercise-induced myoglobinuria

Symptom Information:

Symptom ID: HPO:0008305
Synonyms:
Exercise-induced myoglobinuria in adults [HPO:0008305]
Exercise-induced myoglobinuria in adults [OMIM:Exercise-induced myoglobinuria in adults]
Myoglobinuria, exercise-induced [OMIM:Myoglobinuria, exercise-induced]
Quality:
Cross references:
OMIM: "Exercise-induced myoglobinuria in adults" [OMIM:Exercise-induced myoglobinuria in adults]
OMIM: "Myoglobinuria, exercise-induced" [OMIM:Myoglobinuria, exercise-induced]
Is a (Direct Parents):
HPO         Myoglobinuria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormality of urine homeostasis(HPO:0003110)
                   Myoglobinuria(HPO:0002913)
                      Exercise-induced myoglobinuria(HPO:0008305)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Myoglobinuria(HPO:0002913)
                Exercise-induced myoglobinuria(HPO:0008305)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Glycogen storage disease due to muscle phosphofructokinase deficiency (Orphanet:371)
Glycogen storage disease due to muscle phosphorylase kinase deficiency (Orphanet:715)
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (Orphanet:713)
MYOGLOBINURIA, RECURRENT (OMIM:550500)
Myopathy due to myoadenylate deaminase deficiency (OMIM:615511)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)