Increased intramyocellular lipid droplets
Symptom Information:
Symptom ID: | HPO:0012240 | ||
Synonyms: |
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Quality: | |||
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) Increased intramyocellular lipid droplets(HPO:0012240) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive ataxia due to ubiquinone deficiency | (Orphanet:139485) |
Early-onset spastic ataxia-neuropathy syndrome | (Orphanet:313772) |
Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
Isolated cytochrome C oxidase deficiency | (Orphanet:254905) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
PGM1-CDG | (Orphanet:319646) |