Muscle fiber necrosis
Symptom Information:
Symptom ID: | HPO:0003713 | ||
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) Muscle fiber necrosis(HPO:0003713) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
DPM3-CDG | (Orphanet:263494) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |