Autosomal recessive common variable immunodeficiency due to CR2 mutation

disorder

SNOMED 1351961009CUI C5969672

Overview

Autosomal recessive common variable immunodeficiency due to CR2 mutation is a disorder.

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

Related Conditions

Common variable immunodeficiency(parent)

Hereditary disorder of immune system(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1351961009
UMLS CUI: C5969672
Fully Specified Name: Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation (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 common variable immunodeficiency due to CR2 mutation — Symptoms, Testing & Specialists | Ltrl