Autosomal recessive hereditary arginine vasopressin deficiency

disorder

SNOMED 1296915003CUI C5921858

Overview

Autosomal recessive hereditary arginine vasopressin deficiency is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Hereditary arginine vasopressin-related polyuria(parent)

Hereditary disorder of endocrine system(parent)

Hereditary disorder of nervous system(parent)

Recessive hereditary disorder (autosomal)(parent)

Familial central diabetes insipidus(parent)

Quick Facts

SNOMED CT: 1296915003
UMLS CUI: C5921858
Fully Specified Name: Autosomal recessive hereditary arginine vasopressin deficiency (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.

Autosomal recessive hereditary arginine vasopressin deficiency — Symptoms, Testing & Specialists | Ltrl | Healos