Generalized myoclonic seizures

Symptom Information:

Symptom ID: HPO:0002123
Synonyms:
Myoclonic epilepsy, progressive [HPO:0002123]
Myoclonic seizures [HPO:0002123]
Myoclonus seizures [HPO:0002123]
Myoclonic epilepsy, progressive [OMIM:Myoclonic epilepsy, progressive]
Myoclonic seizures [OMIM:Myoclonic seizures]
Epilepsy, progressive myoclonic [OMIM:Epilepsy, progressive myoclonic]
Myoclonic seizures (1 patient) [OMIM:Myoclonic seizures (1 patient)]
Myoclonic seizures (subtype 3A) [OMIM:Myoclonic seizures (subtype 3A)]
Seizures, myoclonic [OMIM:Seizures, myoclonic]
Quality:
Cross references:
OMIM: "Myoclonic epilepsy, progressive" [OMIM:Myoclonic epilepsy, progressive]
OMIM: "Myoclonic seizures" [OMIM:Myoclonic seizures]
OMIM: "Epilepsy, progressive myoclonic" [OMIM:Epilepsy, progressive myoclonic]
OMIM: "Myoclonic seizures (1 patient)" [OMIM:Myoclonic seizures (1 patient)]
OMIM: "Myoclonic seizures (subtype 3A)" [OMIM:Myoclonic seizures (subtype 3A)]
OMIM: "Seizures, myoclonic" [OMIM:Seizures, myoclonic]
Is a (Direct Parents):
HPO         Generalized seizures
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:
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)