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
Occasional (5-29%)
Shigellosis
Occasional (5-29%)
Langer-Giedion syndrome
Occasional (5-29%)
Globoid cell leukodystrophy, late-onset
Occasional (5-29%)
Childhood absence epilepsy
Occasional (5-29%)
Reye's syndrome
Occasional (5-29%)
Dihydrouracil dehydrogenase (NADP^+^) deficiency
Occasional (5-29%)
Infection by Shigella
Occasional (5-29%)
Deficiency of pyrroline-5-carboxylate reductase
Occasional (5-29%)
Deficiency of guanidinoacetate methyltransferase
Occasional (5-29%)
MCAD deficiency
Occasional (5-29%)
Benign myoclonic epilepsy in infancy
Occasional (5-29%)
Juvenile absence epilepsy
Occasional (5-29%)
Early infantile epileptic encephalopathy with suppression bursts
Occasional (5-29%)
Dravet syndrome
Frequent (30-79%)
Leucocyte adhesion deficiency - type 2
Frequent (30-79%)
3-Methylglutaconic aciduria type 1
Deficiency of prolidase
Frequent (30-79%)
Hyper-IgD periodic fever syndrome
Occasional (5-29%)
Hyperimidodipeptiduria
Frequent (30-79%)
Genetic epilepsy with febrile seizures plus
Frequent (30-79%)
Jeavons syndrome
Occasional (5-29%)
Hyperprolinemia type 2
Occasional (5-29%)
Episodic ataxia type 5
Occasional (5-29%)
Eiken syndrome
Always present (100%)
Quick Facts
- SNOMED CT
- 41497008
- UMLS CUI
- C0009952
- Fully Specified Name
- Febrile convulsion (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.