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.
Hereditary coproporphyria
Occasional (5-29%)
Neuroleptic malignant syndrome
Occasional (5-29%)
Juvenile nephropathic cystinosis
Occasional (5-29%)
Poisoning by colchicine
Frequent (30-79%)
Congenital secretory diarrhea, chloride type
Severe adrenal insufficiency
Frequent (30-79%)
Polycystic kidney disease, infantile type
Frequent (30-79%)
Familial dysautonomia
Occasional (5-29%)
Holoprosencephaly sequence
Occasional (5-29%)
Panhypopituitarism
Occasional (5-29%)
Shigellosis
Occasional (5-29%)
Whipple's disease
Occasional (5-29%)
Cholesterol monooxygenase (side-chain cleaving) deficiency
Frequent (30-79%)
Neurohypophyseal diabetes insipidus
Occasional (5-29%)
Corticosterone 18-monooxygenase deficiency
Always present (100%)
Japanese encephalitis virus disease
Occasional (5-29%)
3 beta-Hydroxysteroid dehydrogenase deficiency
Frequent (30-79%)
Variegate porphyria
Occasional (5-29%)
Poisoning by venomous snake
Very rare (1-4%)
Infantile nephropathic cystinosis
Always present (100%)
Cholera
Frequent (30-79%)
Porphobilinogen synthase deficiency
Occasional (5-29%)
Lowe syndrome
Very frequent (80-99%)
Congenital absence of adrenal gland
Chediak-Higashi syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 89627008
- UMLS CUI
- C0020625
- Fully Specified Name
- Hyponatremia (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.