Status epilepticus

Symptom Information:

Symptom ID: HPO:0002133
Synonyms:
Status epilepticus (disorder) [Orphanet:43390]
Status Epilepticus [Orphanet:43390]
Status epilepticus [OMIM:Status epilepticus]
Seizures/epilepsy/absences/spasms/status epilepticus [Orphanet:43390]
Status epilepticus [Orphanet:43390]
Status epilepticus [MedDRA:10041962]
Epilepsia partialis continua [MedDRA:10041962]
Epilepsia partialis continua, with intractable epilepsy [MedDRA:10041962]
Epilepsia partialis continua, without mention of intractable epilepsy [MedDRA:10041962]
Grand mal status, epileptic [MedDRA:10041962]
Status epilepticus grand mal [MedDRA:10041962]
Nonconvulsive status epilepticus [MedDRA:10041962]
Complex partial status epilepticus [MedDRA:10041962]
Convulsive status epilepticus [MedDRA:10041962]
Epilepsia partialis continua [OMIM:Epilepsia partialis continua]
Status epilepticus (in 1 of 6 patients) [OMIM:Status epilepticus (in 1 of 6 patients)]
Status epilepticus (in some patients) [OMIM:Status epilepticus (in some patients)]
Status epilepticus (in some) [OMIM:Status epilepticus (in some)]
Quality:
Cross references:
Orphanet:43390 "Seizures/epilepsy/absences/spasms/status epilepticus" [Orphanet:43390]
OMIM: "Status epilepticus" [OMIM:Status epilepticus]
OMIM: "Epilepsia partialis continua" [OMIM:Epilepsia partialis continua]
OMIM: "Status epilepticus (in 1 of 6 patients)" [OMIM:Status epilepticus (in 1 of 6 patients)]
OMIM: "Status epilepticus (in some patients)" [OMIM:Status epilepticus (in some patients)]
OMIM: "Status epilepticus (in some)" [OMIM:Status epilepticus (in some)]
UMLS:C0038220 "Status Epilepticus" [Orphanet:43390]
Is a (Direct Parents):
Orphanet Seizures
Orphanet Functional anomalies of the nervous system
HPO         Epilepsia partialis continua
HPO         Seizures
MedDRA Seizures and seizure disorders NEC
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)
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)