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.
Idiopathic hypercalcemia of infancy
Frequent (30-79%)
Diabetes mellitus type I
Familial juvenile gout
Frequent (30-79%)
Infantile nephropathic cystinosis
Frequent (30-79%)
Primary hypomagnesemia
Very frequent (80-99%)
Enamel-renal syndrome
Cystinosis
Frequent (30-79%)
Nephronophthisis
Familial renal glucosuria
Renal dysplasia and retinal aplasia
Frequent (30-79%)
Adolescent nephronophthisis
Frequent (30-79%)
Juvenile nephronophthisis
Maturity-onset diabetes of the young, type 9
Always present (100%)
Hypokalemic alkalosis with hypercalciuria antenatal type 1
Bartter syndrome antenatal type 2
Bartter syndrome type 3
Familial hyperaldosteronism type 3
Occasional (5-29%)
Gitelman's syndrome
Neonatal severe primary hyperparathyroidism
Bartter syndrome type 4a
Always present (100%)
Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
Joubert syndrome with oculorenal defect
Always present (100%)
Autosomal recessive infantile hypercalcaemia
Frequent (30-79%)
Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
Always present (100%)
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
Always present (100%)
Quick Facts
- SNOMED CT
- 28442001
- UMLS CUI
- C0032617
- Fully Specified Name
- Polyuria (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.