Alport syndrome autosomal recessive

disorder

SNOMED 717767009CUI C1567744

Overview

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Alport syndrome(parent)

Quick Facts

SNOMED CT: 717767009
UMLS CUI: C1567744
Fully Specified Name: Alport syndrome autosomal recessive (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.