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.
Tuberous sclerosis syndrome
Frequent (30-79%)
Progressive sclerosing poliodystrophy
Frequent (30-79%)
Cocaine intoxication
Very rare (1-4%)
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
Frequent (30-79%)
Benign Rolandic epilepsy
Cutis verticis gyrata
Occasional (5-29%)
Cysticercosis
Occasional (5-29%)
Niemann-Pick disease, type C
Occasional (5-29%)
Infection by tapeworm larvae
Occasional (5-29%)
Kohlschutter's syndrome
Occasional (5-29%)
Merosin deficient congenital muscular dystrophy
Occasional (5-29%)
Benign neonatal familial convulsions
Very frequent (80-99%)
Lennox-Gastaut syndrome
Occasional (5-29%)
Doose syndrome
Very rare (1-4%)
Lafora disease
Occasional (5-29%)
Early infantile epileptic encephalopathy with suppression bursts
Occasional (5-29%)
Dravet syndrome
Very frequent (80-99%)
Landau-Kleffner syndrome
Frequent (30-79%)
Idiopathic livedo reticularis with systemic involvement
Frequent (30-79%)
Congenital bilateral perisylvian syndrome
Frequent (30-79%)
Genetic epilepsy with febrile seizures plus
Very rare (1-4%)
Subependymal nodular heterotopia
Frequent (30-79%)
Alpha-methylacyl-CoA racemase deficiency disorder
Always present (100%)
Ring chromosome 14
Always present (100%)
Fatty acid hydroxylase associated neurodegeneration
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 29753000
- UMLS CUI
- C0014547
- Fully Specified Name
- Focal onset epileptic seizure (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.