Generalized seizures

Symptom Information:

Symptom ID: HPO:0002197
Synonyms:
Generalized seizures, recurrent [HPO:0002197]
Infrequent generalized seizures [HPO:0002197]
Seizures, generalized, afebrile [HPO:0002197]
Generalized seizures [OMIM:Generalized seizures]
Generalized seizures, recurrent [OMIM:Generalized seizures, recurrent]
Seizures, generalized, afebrile [OMIM:Seizures, generalized, afebrile]
Seizures, generalized [OMIM:Seizures, generalized]
Quality:
Cross references:
OMIM: "Generalized seizures" [OMIM:Generalized seizures]
OMIM: "Generalized seizures, recurrent" [OMIM:Generalized seizures, recurrent]
OMIM: "Seizures, generalized, afebrile" [OMIM:Seizures, generalized, afebrile]
OMIM: "Seizures, generalized" [OMIM:Seizures, generalized]
Is a (Direct Parents):
HPO         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)
MedDRA:
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

Action myoclonus - renal failure syndrome (Orphanet:163696)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Benign familial infantile seizures (Orphanet:306)
CADASIL (Orphanet:136)
Canavan disease (Orphanet:141)
EPILEPSY, IDIOPATHIC GENERALIZED (OMIM:600669)
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10 (OMIM:613060)
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 (OMIM:613832)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 (OMIM:613722)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
Early infantile epileptic encephalopathy without suppression burst (Orphanet:369894)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
Hypouricemia, renal, 2 (OMIM:612076)
Infantile convulsions and choreoathetosis (Orphanet:31709)
Leigh syndrome (Orphanet:506)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MERRF (Orphanet:551)
Malignant migrating partial seizures of infancy (Orphanet:293181)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Ramsay-Hunt syndrome (Orphanet:3020)
Reticular dysgenesis (Orphanet:33355)
SEIZURES, BENIGN FAMILIAL INFANTILE, 1 (OMIM:601764)
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 (OMIM:605751)
Senior-Loken syndrome 7 (OMIM:613615)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)