[DEL]EMG shows myopathic changes

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
HPO:0003458 EMG: myopathic abnormalities [du]
Quality:
Cross references:
OMIM: "EMG shows myopathic changes" [OMIM:EMG shows myopathic changes]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

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 recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive limb-girdle muscular dystrophy type 2B (Orphanet:268)
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)
Distal myopathy with early respiratory muscle involvement (Orphanet:34521)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE (OMIM:600737)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 (OMIM:606612)
MYOPATHY, DISTAL, 3 (OMIM:610099)
MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE (OMIM:255160)
Marinesco-Sjögren syndrome (Orphanet:559)
Mitochondrial DNA depletion syndrome, myopathic form (Orphanet:254875)
Myopathy and diabetes mellitus (Orphanet:2596)
NEMALINE MYOPATHY 1 (OMIM:609284)
NEMALINE MYOPATHY 6 (OMIM:609273)
NONAKA MYOPATHY (OMIM:605820)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 2 (OMIM:609283)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
ZASP-related myofibrillar myopathy (Orphanet:98912)