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.
Fragile X syndrome
Gestational rubella syndrome
Occasional (5-29%)
Dubowitz's syndrome
Occasional (5-29%)
Pigmentary pallidal degeneration
Very rare (1-4%)
Ruvalcaba syndrome
Occasional (5-29%)
Listeriosis
Occasional (5-29%)
Hypertyrosinemia, Richner-Hanhart type
Occasional (5-29%)
Bardet-Biedl syndrome
Occasional (5-29%)
Subacute neuronopathic Gaucher's disease
Frequent (30-79%)
Hyperleucine-isoleucinemia
Tuberous sclerosis syndrome
Very frequent (80-99%)
Glycogen storage disease, type I
Very frequent (80-99%)
Hereditary coproporphyria
Occasional (5-29%)
Classical phenylketonuria
Septo-optic dysplasia sequence
Frequent (30-79%)
Biotinidase deficiency
Frequent (30-79%)
Crigler-Najjar syndrome, type I
Occasional (5-29%)
Killian-Teschler-Nicola syndrome
Frequent (30-79%)
Coffin-Siris syndrome
Frequent (30-79%)
Lesch-Nyhan syndrome
Occasional (5-29%)
Polyglandular autoimmune syndrome, type 1
Occasional (5-29%)
Acute neuronopathic Gaucher's disease
Frequent (30-79%)
Periodic disease
Frequent (30-79%)
Cystathioninuria
Frequent (30-79%)
Methylcrotonyl-CoA carboxylase deficiency
Quick Facts
- SNOMED CT
- 91175000
- UMLS CUI
- C0036572
- Fully Specified Name
- 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.