Generalized tonic-clonic seizures
Symptom Information:
Symptom ID: | HPO:0002069 | |||||||||||||||||||||||||
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 tonic-clonic seizures(HPO:0002069) MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Generalized tonic-clonic seizures(HPO:0002069) |
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Database Frequency: | 96 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
4-hydroxybutyric aciduria | (Orphanet:22) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Alopecia - intellectual deficit - hypergonadotropic hypogonadism | (Orphanet:1014) |
Alström syndrome | (Orphanet:64) |
Alternating hemiplegia of childhood | (Orphanet:2131) |
Amish infantile epilepsy syndrome | (Orphanet:171714) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Benign adult familial myoclonic epilepsy | (Orphanet:86814) |
Benign familial neonatal seizures | (Orphanet:1949) |
Beta-mannosidosis | (Orphanet:118) |
Bilateral polymicrogyria | (Orphanet:268940) |
Childhood absence epilepsy | (Orphanet:64280) |
Christianson syndrome | (Orphanet:85278) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1 | (OMIM:600131) |
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 | (OMIM:607681) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 | (OMIM:607876) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3 | (OMIM:613608) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4 | (OMIM:615127) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5 | (OMIM:615400) |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 | (OMIM:608096) |
EPILEPSY, IDIOPATHIC GENERALIZED | (OMIM:600669) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10 | (OMIM:613060) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 | (OMIM:614847) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3 | (OMIM:608762) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7 | (OMIM:604827) |
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9 | (OMIM:614280) |
EPILEPSY, MYOCLONIC JUVENILE | (OMIM:254770) |
EPILEPSY, NOCTURNAL FRONTAL LOBE, 2 | (OMIM:603204) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 1B | (OMIM:612437) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 8 | (OMIM:616230) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 | (OMIM:613721) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 | (OMIM:616341) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
Early-onset spastic ataxia-neuropathy syndrome | (Orphanet:313772) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
FEBRILE SEIZURES, FAMILIAL, 1 | (OMIM:121210) |
FEBRILE SEIZURES, FAMILIAL, 11 | (OMIM:614418) |
FEBRILE SEIZURES, FAMILIAL, 2 | (OMIM:602477) |
FEBRILE SEIZURES, FAMILIAL, 4 | (OMIM:604352) |
FEBRILE SEIZURES, FAMILIAL, 5 | (OMIM:609255) |
FEBRILE SEIZURES, FAMILIAL, 6 | (OMIM:609253) |
Familial infantile myoclonic epilepsy | (Orphanet:352582) |
Familial temporal epilepsy | (Orphanet:98819) |
Female restricted epilepsy with intellectual deficit | (Orphanet:101039) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 | (OMIM:604233) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 | (OMIM:604403) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 | (OMIM:611277) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4 | (OMIM:609800) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7 | (OMIM:613863) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9 | (OMIM:616172) |
GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY | (OMIM:608278) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 3 | (Orphanet:77261) |
Generalized epilepsy - paroxysmal dyskinesia | (Orphanet:79137) |
Generalized epilepsy with febrile seizures-plus context | (Orphanet:36387) |
Glycogen storage disease due to muscle and heart glycogen synthase deficiency | (Orphanet:137625) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hypouricemia, renal, 1 | (OMIM:220150) |
Juvenile absence epilepsy | (Orphanet:1941) |
Juvenile myoclonic epilepsy | (Orphanet:307) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
Lafora disease | (Orphanet:501) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49 | (OMIM:616281) |
MERRF | (Orphanet:551) |
MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C | (OMIM:615501) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 | (OMIM:257300) |
MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG | (OMIM:254800) |
MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4 | (OMIM:611364) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Occipital pachygyria and polymicrogyria | (Orphanet:280640) |
PELGER-HUET ANOMALY | (OMIM:169400) |
Pachygyria - intellectual deficit - epilepsy | (Orphanet:2798) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Perrault Syndrome 5 | (OMIM:616138) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |
Progressive myoclonic epilepsy type 6 | (Orphanet:280620) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 | (OMIM:121200) |
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 | (OMIM:121201) |
SEIZURES, BENIGN FAMILIAL NEONATAL, 3 | (OMIM:608217) |
SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE | (OMIM:269720) |
Sneddon syndrome | (Orphanet:820) |
Unverricht-Lundborg disease | (Orphanet:308) |
X-linked intellectual disability, Hedera type | (Orphanet:93952) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |