Autosomal dominant combined immunodeficiency due to ERBIN deficiency

disorder

SNOMED 1351324009CUI C5925110

Overview

Autosomal dominant combined immunodeficiency due to ERBIN deficiency is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hyperimmunoglobulin E syndrome(parent)

Quick Facts

SNOMED CT: 1351324009
UMLS CUI: C5925110
Fully Specified Name: Autosomal dominant combined immunodeficiency due to erbb2 interacting protein deficiency (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.