Exercise-induced myalgia

Symptom Information:

Symptom ID: HPO:0003738
Synonyms:
Exercise-induced muscle pain [HPO:0003738]
Muscle pain on exercise [HPO:0003738]
Muscle pain with exercise [HPO:0003738]
Muscle pain, exercise-induced [HPO:0003738]
Exercise-induced muscle pain [OMIM:Exercise-induced muscle pain]
Exercise-induced myalgia [OMIM:Exercise-induced myalgia]
Muscle pain with exercise [OMIM:Muscle pain with exercise]
Muscle pain, exercise-induced [OMIM:Muscle pain, exercise-induced]
Muscle pain with exercise (in older patients) [OMIM:Muscle pain with exercise (in older patients)]
Quality:
Cross references:
OMIM: "Exercise-induced muscle pain" [OMIM:Exercise-induced muscle pain]
OMIM: "Exercise-induced myalgia" [OMIM:Exercise-induced myalgia]
OMIM: "Muscle pain with exercise" [OMIM:Muscle pain with exercise]
OMIM: "Muscle pain, exercise-induced" [OMIM:Muscle pain, exercise-induced]
OMIM: "Muscle pain with exercise (in older patients)" [OMIM:Muscle pain with exercise (in older patients)]
Is a (Direct Parents):
HPO         Myalgia
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)