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.
Biotinidase deficiency
Occasional (5-29%)
Killian-Teschler-Nicola syndrome
Cocaine intoxication
Very rare (1-4%)
Fructose-biphosphatase deficiency
Childhood absence epilepsy
Occasional (5-29%)
Cholera
Occasional (5-29%)
Encephalitis lethargica
Occasional (5-29%)
Acute liver failure
Occasional (5-29%)
Fulminant hepatic failure
Occasional (5-29%)
Holocarboxylase synthase deficiency
ADNFLE - Autosomal dominant nocturnal frontal lobe epilepsy
Occasional (5-29%)
Pitt-Hopkins syndrome
Frequent (30-79%)
Chronic pneumonitis of infancy
Frequent (30-79%)
Maternally inherited Leigh syndrome
Occasional (5-29%)
CDKL5 deficiency disorder
Occasional (5-29%)
Adult-onset cervical dystonia DYT23 type
Occasional (5-29%)
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 68978004
- UMLS CUI
- C0020578
- Fully Specified Name
- Hyperventilation (finding)
- Associated Conditions
- 17
- 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.