Status epilepticus
Symptom Information:
Symptom ID: | HPO:0002133 | ||||||||||||||||||
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) Status epilepticus(HPO:0002133) MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Seizures and seizure disorders NEC(MedDRA:10039912) Status epilepticus(HPO:0002133) |
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Database Frequency: | 59 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
4-hydroxybutyric aciduria | (Orphanet:22) |
48,XXYY syndrome | (Orphanet:10) |
ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY | (OMIM:614307) |
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 | (OMIM:614820) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Alpers syndrome | (Orphanet:726) |
Alström syndrome | (Orphanet:64) |
Amish infantile epilepsy syndrome | (Orphanet:171714) |
Argininemia | (Orphanet:90) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Bangstad syndrome | (Orphanet:1227) |
Beta-ureidopropionase deficiency | (Orphanet:65287) |
CADASIL | (Orphanet:136) |
CLN10 disease | (Orphanet:228337) |
COENZYME Q10 DEFICIENCY, PRIMARY, 3 | (OMIM:614652) |
COG8-CDG | (Orphanet:95428) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Classical phenylketonuria | (Orphanet:79254) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
Dravet syndrome | (Orphanet:33069) |
EPILEPSY, NOCTURNAL FRONTAL LOBE, 2 | (OMIM:603204) |
EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 | (OMIM:615005) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 | (OMIM:613721) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | (OMIM:614959) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19 | (OMIM:615744) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25 | (OMIM:615905) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
Female restricted epilepsy with intellectual deficit | (Orphanet:101039) |
Fumaric aciduria | (Orphanet:24) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
HERNS syndrome | (Orphanet:63261) |
Hyperprolinemia type 1 | (Orphanet:419) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Juvenile myoclonic epilepsy | (Orphanet:307) |
Leigh syndrome | (Orphanet:506) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLARATROPHY | (OMIM:615760) |
Maple syrup urine disease | (Orphanet:511) |
Menkes disease | (Orphanet:565) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Niemann-Pick disease type C | (Orphanet:646) |
POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL | (OMIM:612691) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Progressive myoclonic epilepsy with dystonia | (Orphanet:352596) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
Tyrosinemia type 2 | (Orphanet:28378) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolfram syndrome | (Orphanet:3463) |