Type 1 and type 2 muscle fiber minicore regions
Symptom Information:
| Symptom ID: | HPO:0003787 | ||
| Synonyms: |
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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) Myopathy(HPO:0003198) Minicore myopathy(HPO:0003789) Type 1 and type 2 muscle fiber minicore regions(HPO:0003787) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
| Classic multiminicore myopathy | (Orphanet:324604) |
| Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |