Type 1 fiber predominance
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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HPO:
MedDRA: |
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| Database Frequency: | 9 / 7739 | |
| Resource: |
All diseases associated with this symptom:
| Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
| Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
| Distal myopathy with posterior leg and anterior hand involvement | (Orphanet:63273) |
| Early-onset myopathy with fatal cardiomyopathy | (Orphanet:289377) |
| Laing distal myopathy | (Orphanet:59135) |
| MYOPATHY, CENTRONUCLEAR, 1 | (OMIM:160150) |
| Marinesco-Sjögren syndrome | (Orphanet:559) |
| NEMALINE MYOPATHY 7 | (OMIM:610687) |
| X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |