Generalized seizures
Symptom Information:
Symptom ID: | HPO:0002197 | |||||||
Synonyms: |
|
|||||||
Quality: | ||||||||
Cross references: |
|
|||||||
Is a (Direct Parents): |
|
|||||||
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) |