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Hereditary arginine vasopressin-related polyuria
disorderSNOMED 1296911007CUI C5921856
Overview
Hereditary arginine vasopressin-related polyuria is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Hereditary vasopressin resistance(child)
Autosomal dominant hereditary arginine vasopressin deficiency(child)
Autosomal recessive hereditary arginine vasopressin deficiency(child)
X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome(child)
Vasopressin-related polyuria(parent)
Hereditary disease(parent)
Quick Facts
- SNOMED CT
- 1296911007
- UMLS CUI
- C5921856
- Fully Specified Name
- Hereditary arginine vasopressin-related polyuria (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.