Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation

disorder

SNOMED 1354596000CUI C5969793

Overview

Autosomal recessive common variable immunodeficiency due to POU2AF1 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: 1354596000
UMLS CUI: C5969793
Fully Specified Name: Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 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.