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.
Neuroleptic malignant syndrome
Occasional (5-29%)
Postencephalitic parkinsonism
Frequent (30-79%)
Tetrahydrobiopterin synthesis defect
Occasional (5-29%)
Deficiency of tryptophan decarboxylase
Frequent (30-79%)
6-Pyruvoyl-tetrahydrobiopterin synthase deficiency
Occasional (5-29%)
Autosomal recessive dopa responsive dystonia
Frequent (30-79%)
Limbic encephalitis with N-methyl-D-aspartate receptor antibodies
Occasional (5-29%)
Brain dopamine-serotonin vesicular transport disease
Very frequent (80-99%)
Dopamine transporter deficiency syndrome
Frequent (30-79%)
Kufor Rakeb syndrome
Frequent (30-79%)
Bilateral generalized polymicrogyria
Occasional (5-29%)
Dopa responsive dystonia due to sepiapterin reductase deficiency
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 5332004
- UMLS CUI
- C0085637
- Fully Specified Name
- Oculogyric crisis (finding)
- Associated Conditions
- 12
- 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.