Autosomal dominant hyper IgM syndrome due to AICDA

disorder

SNOMED 1351570003CUI C5968779

Overview

Autosomal dominant hyper IgM syndrome due to AICDA is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hyper-IgM syndrome without susceptibility to opportunistic infections(parent)

Quick Facts

SNOMED CT: 1351570003
UMLS CUI: C5968779
Fully Specified Name: Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase 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.