EMG: myopathic abnormalities

Symptom Information:

Symptom ID: HPO:0003458
Synonyms:
EMG: myopathic changes [HPO:0003458]
EMG: myopathy [HPO:0003458]
Myopathic electromyogram [HPO:0003458]
Myopathic changes seen on EMG [OMIM,du]
EMG shows myopathic changes [OMIM,du]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Myopathy
HPO         EMG abnormality
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:
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)