Autosomal recessive common variable immunodeficiency due to CD20 mutation

disorder

SNOMED 1351960005CUI C5969671

Overview

Autosomal recessive common variable immunodeficiency due to CD20 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: 1351960005
UMLS CUI: C5969671
Fully Specified Name: Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 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 CD20 mutation — Symptoms, Testing & Specialists | Ltrl