Increased muscle lipid content
Symptom Information:
Symptom ID: | HPO:0009058 | ||||||
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) Increased muscle lipid content(HPO:0009058) MedDRA: |
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Database Frequency: | 6 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Neutral lipid storage myopathy | (Orphanet:98908) |