Muscle fiber inclusion bodies
Symptom Information:
| Symptom ID: | HPO:0100299 | ||
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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) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| AMYOTROPHIC LATERAL SCLEROSIS 20 | (OMIM:615426) |
| Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia | (Orphanet:79091) |
| INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 3 | (OMIM:615424) |