Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency

disorder

SNOMED 1354420003CUI C5969708

Overview

Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Common variable immunodeficiency(parent)

Hereditary disorder of immune system(parent)

Quick Facts

SNOMED CT: 1354420003
UMLS CUI: C5969708
Fully Specified Name: Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 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.