Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation

disorder

SNOMED 1354472008CUI C5969723

Overview

Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation is a disorder.

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

Related Conditions

Common variable immunodeficiency(parent)

Hereditary disorder of immune system(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1354472008
UMLS CUI: C5969723
Fully Specified Name: Autosomal recessive combined variable immunodeficiency due to Rho guanine nucleotide exchange factor 1 mutation (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 recessive combined variable immunodeficiency due to ARHGEF1 mutation — Symptoms, Testing & Specialists | Ltrl