Alport syndrome autosomal dominant

disorder

SNOMED 717766000CUI C1567743

Overview

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Alport syndrome(parent)

Quick Facts

SNOMED CT: 717766000
UMLS CUI: C1567743
Fully Specified Name: Alport syndrome autosomal dominant (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.