Autosomal recessive agammaglobulinaemia due to IGHM mutation

disorder

SNOMED 1351675000CUI C5968881

Overview

Autosomal recessive agammaglobulinaemia due to IGHM mutation is a disorder.

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

Related Conditions

Autosomal recessive agammaglobulinemia(parent)

Quick Facts

SNOMED CT: 1351675000
UMLS CUI: C5968881
Fully Specified Name: Autosomal recessive agammaglobulinemia due to immunoglobulin heavy chain mu constant region 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.