Generalized myoclonic seizures
Symptom Information:
Symptom ID: | HPO:0002123 | |||||||||
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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Seizures(HPO:0001250) Generalized seizures(HPO:0002197) Generalized myoclonic seizures(HPO:0002123) MedDRA: |
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Database Frequency: | 62 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
4-hydroxybutyric aciduria | (Orphanet:22) |
ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA | (OMIM:208700) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Alpers syndrome | (Orphanet:726) |
Atypical Rett syndrome | (Orphanet:3095) |
Benign adult familial myoclonic epilepsy | (Orphanet:86814) |
CLN11 disease | (Orphanet:314629) |
CLN7 disease | (Orphanet:228366) |
Carnosinemia | (Orphanet:1361) |
Combined immunodeficiency with facio-oculo-skeletal anomalies | (Orphanet:221139) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Congenital ichthyosis - intellectual deficit - spastic quadriplegia | (Orphanet:352333) |
DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY | (OMIM:220300) |
Dravet syndrome | (Orphanet:33069) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5 | (OMIM:615400) |
EPILEPSY, IDIOPATHIC GENERALIZED | (OMIM:600669) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10 | (OMIM:613060) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11 | (OMIM:607628) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3 | (OMIM:608762) |
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9 | (OMIM:614280) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 1B | (OMIM:612437) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 | (OMIM:613832) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 | (OMIM:616341) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
Early infantile epileptic encephalopathy | (Orphanet:1934) |
Early myoclonic encephalopathy | (Orphanet:1935) |
Early-onset spastic ataxia-neuropathy syndrome | (Orphanet:313772) |
Familial encephalopathy with neuroserpin inclusion bodies | (Orphanet:85110) |
Familial infantile myoclonic epilepsy | (Orphanet:352582) |
Farber lipogranulomatosis | (Orphanet:333) |
Female restricted epilepsy with intellectual deficit | (Orphanet:101039) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 | (OMIM:604403) |
GM1 gangliosidosis type 2 | (Orphanet:79256) |
Gaucher disease type 3 | (Orphanet:77261) |
HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT | (OMIM:235830) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Infantile epileptic-dyskinetic encephalopathy | (Orphanet:364063) |
Juvenile absence epilepsy | (Orphanet:1941) |
Lafora disease | (Orphanet:501) |
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY | (OMIM:606369) |
MENTAL RETARDATION, X-LINKED 89 | (OMIM:300848) |
MERRF | (Orphanet:551) |
MICROCEPHALY WITH SPASTIC QUADRIPLEGIA | (OMIM:251280) |
MICROHYDRANENCEPHALY | (OMIM:605013) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 | (OMIM:257300) |
MYOCLONIC EPILEPSY, HARTUNG TYPE | (OMIM:159600) |
MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4 | (OMIM:611364) |
MYOCLONIC EPILEPSY, PROGRESSIVE | (OMIM:310370) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
PAINE SYNDROME | (OMIM:311400) |
Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome | (Orphanet:306558) |
Progressive myoclonic epilepsy type 3 | (Orphanet:263516) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL | (OMIM:614498) |
Seizures - intellectual deficit due to hydroxylysinuria | (Orphanet:79156) |
Spasticity - intellectual deficit - X-linked epilepsy | (Orphanet:3175) |