Skeletal myopathy
Symptom Information:
| Symptom ID: | HPO:0003756 | ||
| 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) Skeletal myopathy(HPO:0003756) MedDRA: |
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| Database Frequency: | 8 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Barth syndrome | (Orphanet:111) |
| Cardiomyopathy, familial hypertrophic, 8 | (OMIM:608751) |
| Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
| Carnitine uptake deficiency | (Orphanet:158) |
| Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
| Desminopathy | (Orphanet:98909) |
| Histiocytoid cardiomyopathy | (Orphanet:137675) |
| Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |