EMG abnormality

Symptom Information:

Symptom ID: HPO:0003457
Abnormal electromyography finding [HPO:0003457]
Abnormal EMG [HPO:0003457]
Electromyogram abnormal [HPO:0003457]
EMG abnormalities [HPO:0003457]
Electromyogram abnormal (finding) [Orphanet:44700]
Electromyogram abnormal [Orphanet:44700]
Abnormal EMG [OMIM:Abnormal EMG]
Electromyogram abnormal [OMIM:Electromyogram abnormal]
Abnormal EMG/electromyogram/electropmyography [Orphanet:44700]
Electromyogram abnormal [MedDRA:10014431]
Abnormal EMG [MedDRA:10014431]
EMG abnormal [MedDRA:10014431]
Muscular contraction wave abnormal [MedDRA:10014431]
Nonspecific abnormal electromyogram (EMG) [MedDRA:10014431]
Anal sphincter electromyography abnormal [MedDRA:10014431]
Presence of abnormal F wave on EMG [MedDRA:10014431]
Cross references:
Orphanet:44700 "Abnormal EMG/electromyogram/electropmyography" [Orphanet:44700]
OMIM: "Abnormal EMG" [OMIM:Abnormal EMG]
OMIM: "Electromyogram abnormal" [OMIM:Electromyogram abnormal]
UMLS:C0476403 "Electromyogram abnormal" [Orphanet:44700]
Is a (Direct Parents):
Orphanet Muscle anomalies
HPO         Single fiber EMG abnormality
HPO         EMG: repetitive nerve stimulation abnormality
HPO         Abnormality of muscle physiology
MedDRA Neurologic diagnostic procedures
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             EMG abnormality(HPO:0003457)
    Neurological, special senses and psychiatric investigations(MedDRA:10029295)
       Neurologic diagnostic procedures(MedDRA:10029285)
          EMG abnormality(HPO:0003457)
Database Frequency: 78 / 7739

All diseases associated with this symptom:

Acetazolamide-responsive myotonia (Orphanet:99736)
Adrenomyodystrophy (Orphanet:977)
Adult polyglucosan body disease (Orphanet:206583)
Antisynthetase syndrome (Orphanet:81)
Apolipoprotein A-I deficiency (Orphanet:425)
Arthrogryposis due to muscular dystrophy (Orphanet:1155)
Ataxia-deafness-retardation syndrome (Orphanet:1188)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal recessive limb-girdle muscular dystrophy type 2H (Orphanet:1878)
Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
Bethlem myopathy (Orphanet:610)
Centronuclear myopathy (Orphanet:595)
Cervical hypertrichosis - peripheral neuropathy (Orphanet:2218)
Charcot-Marie-Tooth disease (Orphanet:166)
Choreoacanthocytosis (Orphanet:2388)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
Deafness - small bowel diverticulosis - neuropathy (Orphanet:3217)
Dermatomyositis (Orphanet:221)
Duchenne and Becker muscular dystrophy (Orphanet:262)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Facioscapulohumeral dystrophy (Orphanet:269)
Familial dysautonomia (Orphanet:1764)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Gemignani syndrome (Orphanet:2074)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Gyrate atrophy of choroid and retina (Orphanet:414)
Hereditary continuous muscle fiber activity (Orphanet:972)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
Hyperkalemic periodic paralysis (Orphanet:682)
Hypomyelination neuropathy - arthrogryposis (Orphanet:2680)
Inclusion body myositis (Orphanet:611)
Isolated glycerol kinase deficiency (Orphanet:408)
Juvenile amyotrophic lateral sclerosis (Orphanet:300605)
Juvenile dermatomyositis (Orphanet:93672)
Kearns-Sayre syndrome (Orphanet:480)
Krabbe disease (Orphanet:487)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
Macrophagic myofasciitis (Orphanet:592)
Marden-Walker syndrome (Orphanet:2461)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Mitochondrial myopathy - lactic acidosis - deafness (Orphanet:2597)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Monomelic amyotrophy (Orphanet:65684)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Muscle-eye-brain disease (Orphanet:588)
Muscular dystrophy - white matter spongiosis (Orphanet:1877)
Myhre syndrome (Orphanet:2588)
Myoclonus - cerebellar ataxia - deafness (Orphanet:2589)
Myotonia fluctuans (Orphanet:99734)
Myotonia permanens (Orphanet:99735)
Neuralgic amyotrophy (Orphanet:2901)
Neurogenic thoracic outlet syndrome (Orphanet:100073)
Neuronal intranuclear inclusion disease (Orphanet:2289)
Neutral lipid storage disease (Orphanet:165)
O'Sullivan-McLeod syndrome (Orphanet:99965)
Palmoplantar keratoderma-spastic paralysis syndrome (Orphanet:2201)
Peripheral motor neuropathy - dysautonomia (Orphanet:2400)
Polymyositis (Orphanet:732)
Polyneuropathy - intellectual deficit - acromicria - premature menopause (Orphanet:2928)
Potassium-aggravated myotonia (Orphanet:612)
Primary orthostatic tremor (Orphanet:238606)
Proximal spinal muscular atrophy (Orphanet:70)
Proximal spinal muscular atrophy type 2 (Orphanet:83418)
Proximal spinal muscular atrophy type 3 (Orphanet:83419)
Rippling muscle disease (Orphanet:97238)
Schwartz-Jampel syndrome (Orphanet:800)
Spastic ataxia - corneal dystrophy (Orphanet:2572)
Spinocerebellar ataxia - dysmorphism (Orphanet:1185)
Steinert myotonic dystrophy (Orphanet:273)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Thomsen and Becker disease (Orphanet:614)
Thoracic outlet syndrome (Orphanet:97330)
Usher syndrome (Orphanet:886)
X-linked centronuclear myopathy (Orphanet:596)