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.

Autosomal dominant hyper IgM syndrome due to AICDA — Symptoms, Testing & Specialists | Ltrl | Ltrl