Exercise intolerance

Symptom Information:

Symptom ID: HPO:0003546
Synonyms:
Exercise intolerance [OMIM:Exercise intolerance]
Exercise intolerance (CVS+) [OMIM:Exercise intolerance (CVS+)]
Exercise intolerance (also seen in some heterozygotes) [OMIM:Exercise intolerance (also seen in some heterozygotes)]
Exercise intolerance (less common) [OMIM:Exercise intolerance (less common)]
Exercise tolerance decreased [MedDRA:10051301, cm]
Quality:
Cross references:
OMIM: "Exercise intolerance" [OMIM:Exercise intolerance]
OMIM: "Exercise intolerance (CVS+)" [OMIM:Exercise intolerance (CVS+)]
OMIM: "Exercise intolerance (also seen in some heterozygotes)" [OMIM:Exercise intolerance (also seen in some heterozygotes)]
OMIM: "Exercise intolerance (less common)" [OMIM:Exercise intolerance (less common)]
Is a (Direct Parents):
HPO         Functional motor problems
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:
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)