Exercise intolerance
Symptom Information:
Symptom ID: | HPO:0003546 | |||||
Synonyms: |
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Cross references: |
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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 physiology(HPO:0011804) Functional motor problems(HPO:0004302) Exercise intolerance(HPO:0003546) MedDRA: |
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Database Frequency: | 62 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
ATTRV122I amyloidosis | (Orphanet:85451) |
Acute interstitial pneumonia | (Orphanet:79126) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive ataxia due to ubiquinone deficiency | (Orphanet:139485) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2T | (Orphanet:363623) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Barth syndrome | (Orphanet:111) |
Becker muscular dystrophy | (Orphanet:98895) |
CILIARY DYSKINESIA, PRIMARY, 11 | (OMIM:612649) |
CILIARY DYSKINESIA, PRIMARY, 12 | (OMIM:612650) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Cardiomyopathy, familial restrictive, 3 | (OMIM:612422) |
Desminopathy | (Orphanet:98909) |
Fabry disease | (Orphanet:324) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
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 and heart glycogen synthase deficiency | (Orphanet:137625) |
Glycogen storage disease due to muscle beta-enolase deficiency | (Orphanet:99849) |
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 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) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isolated cytochrome C oxidase deficiency | (Orphanet:254905) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Left ventricular noncompaction | (Orphanet:54260) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE) | (OMIM:615418) |
MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT | (OMIM:251945) |
MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT | (OMIM:616209) |
Maternally-inherited cardiomyopathy and hearing loss | (Orphanet:1349) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Myopathy due to myoadenylate deaminase deficiency | (OMIM:615511) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
Neutral lipid storage myopathy | (Orphanet:98908) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 2 | (OMIM:609283) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 | (OMIM:610131) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 | (OMIM:613077) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Pulmonary nodular lymphoid hyperplasia | (Orphanet:60026) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Pyruvate dehydrogenase phosphatase deficiency | (Orphanet:79246) |
Scheie syndrome | (Orphanet:93474) |
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | (Orphanet:206546) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |