Muscle fiber cytoplasmatic inclusion bodies
Symptom Information:
| Symptom ID: | HPO:0100303 | ||
| Synonyms: |
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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 inclusion bodies(HPO:0100299) Muscle fiber cytoplasmatic inclusion bodies(HPO:0100303) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
| Muscle filaminopathy | (Orphanet:171445) |
| Myotilin-related myofibrillar myopathy without spheroid body | (Orphanet:98911) |