Autosomal dominant agammaglobulinaemia due to E47 transcription factor deficiency

disorder

SNOMED 1351668001CUI C5968876

Overview

Autosomal dominant agammaglobulinaemia due to E47 transcription factor deficiency is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Isolated agammaglobulinaemia(parent)

Quick Facts

SNOMED CT: 1351668001
UMLS CUI: C5968876
Fully Specified Name: Autosomal dominant agammaglobulinemia due to E47 transcription factor 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.