EMG: myopathic abnormalities
Symptom Information:
Symptom ID: | HPO:0003458 | |||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) EMG: myopathic abnormalities(HPO:0003458) Abnormality of muscle physiology(HPO:0011804) EMG abnormality(HPO:0003457) EMG: myopathic abnormalities(HPO:0003458) MedDRA: |
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Database Frequency: | 38 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
ATTRV122I amyloidosis | (Orphanet:85451) |
Alpha-crystallinopathy | (Orphanet:98910) |
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Autosomal recessive limb-girdle muscular dystrophy type 2J | (Orphanet:140922) |
Autosomal recessive limb-girdle muscular dystrophy type 2L | (Orphanet:206549) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Cap myopathy | (Orphanet:171881) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Desminopathy | (Orphanet:98909) |
Distal myopathy with early respiratory muscle involvement | (Orphanet:34521) |
Distal myopathy, Nonaka type | (Orphanet:602) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Hyaline body myopathy | (Orphanet:53698) |
MERRF | (Orphanet:551) |
MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEMATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS | (OMIM:601170) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 | (OMIM:608840) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
MYOPATHY, MYOSIN STORAGE | (OMIM:608358) |
Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Myopathy and diabetes mellitus | (Orphanet:2596) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NONAKA MYOPATHY | (OMIM:605820) |
Nemaline myopathy | (Orphanet:607) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 2 | (OMIM:609283) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
SCAPULOPERONEAL MYOPATHY, MYH7-RELATED | (OMIM:181430) |
Tibial muscular dystrophy | (Orphanet:609) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |