Fatty replacement of skeletal muscle
Symptom Information:
| Symptom ID: | HPO:0012548 | ||
| 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) Fatty replacement of skeletal muscle(HPO:0012548) MedDRA: |
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| Database Frequency: | 8 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
| Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
| Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
| Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
| Congenital muscular dystrophy with integrin alpha-7 deficiency | (Orphanet:34520) |
| Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
| MERRF | (Orphanet:551) |
| MYOPATHY WITH ABNORMAL LIPID METABOLISM | (OMIM:255100) |