Familial idiopathic hypercalciuria

disorder

SNOMED 237886009CUI C0342639

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Ca2+ oxalate urolithiasis

HP:0008672

Hypercalciuria

HP:0002150

Related Conditions

Hypercalciuria(parent)

Idiopathic disease(parent)

Familial disease(parent)

Quick Facts

SNOMED CT: 237886009
UMLS CUI: C0342639
Fully Specified Name: Familial idiopathic hypercalciuria (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 2

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.