Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Juvenile myoclonic epilepsy
Tuberous sclerosis syndrome
Frequent (30-79%)
Yellow fever
Very rare (1-4%)
Progressive sclerosing poliodystrophy
Frequent (30-79%)
Cocaine intoxication
Very rare (1-4%)
Leigh's disease
Very rare (1-4%)
Succinate-semialdehyde dehydrogenase deficiency
Frequent (30-79%)
Japanese encephalitis virus disease
Occasional (5-29%)
Cysticercosis
Occasional (5-29%)
Hemiplegic migraine
Very rare (1-4%)
Proline dehydrogenase deficiency
Niemann-Pick disease, type C
Very rare (1-4%)
Angelman syndrome
Occasional (5-29%)
Infection by tapeworm larvae
Occasional (5-29%)
Deficiency of pyrroline-5-carboxylate reductase
Occasional (5-29%)
Deficiency of glycerate kinase
Frequent (30-79%)
Deficiency of beta-ureidopropionase
Occasional (5-29%)
Benign neonatal familial convulsions
Very rare (1-4%)
Juvenile absence epilepsy
Occasional (5-29%)
Lafora disease
Frequent (30-79%)
Dravet syndrome
Alternating hemiplegia of childhood
Occasional (5-29%)
D-Glyceric aciduria
Frequent (30-79%)
Fumarase deficiency
WSS - Wrinkly skin syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 230456007
- UMLS CUI
- C0038220
- Fully Specified Name
- Status epilepticus (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.