Exercise-induced myalgia
Symptom Information:
Symptom ID: | HPO:0003738 | |||||||||
Synonyms: |
|
|||||||||
Quality: | ||||||||||
Cross references: |
|
|||||||||
Is a (Direct Parents): |
|
|||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Myalgia(HPO:0003326) Exercise-induced myalgia(HPO:0003738) MedDRA: |
|||||||||
Database Frequency: | 19 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Glycogen storage disease due to muscle glycogen phosphorylase deficiency | (Orphanet:368) |
Glycogen storage disease due to muscle phosphorylase kinase deficiency | (Orphanet:715) |
Glycogen storage disease due to phosphoglycerate mutase deficiency | (Orphanet:97234) |
Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT | (OMIM:254960) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Myopathy due to myoadenylate deaminase deficiency | (OMIM:615511) |
PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA | (OMIM:600706) |
RIPPLING MUSCLE DISEASE | (OMIM:606072) |
RIPPLING MUSCLE DISEASE 1 | (OMIM:600332) |
Rippling muscle disease | (Orphanet:97238) |
Scheie syndrome | (Orphanet:93474) |
Tubular aggregate myopathy | (Orphanet:2593) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |