Increased muscle glycogen content
Symptom Information:
Symptom ID: | HPO:0009051 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 morphology(HPO:0011805) Abnormality of muscle fibers(HPO:0004303) Abnormal muscle glycogen content(HPO:0012269) Increased muscle glycogen content(HPO:0009051) MedDRA: |
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Database Frequency: | 8 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Cardiomyopathy, familial hypertrophic, 6 | (OMIM:600858) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
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 phosphorylase kinase deficiency | (Orphanet:370) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
PGM1-CDG | (Orphanet:319646) |