Autosomal recessive CVID (combined variable immunodeficiency) due to PIK3CG deficiency

disorder

SNOMED 1354483004CUI C5969731

Overview

Autosomal recessive CVID (combined variable immunodeficiency) due to PIK3CG deficiency 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: 1354483004
UMLS CUI: C5969731
Fully Specified Name: Autosomal recessive combined variable immunodeficiency due to phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma 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 CVID (combined variable immunodeficiency) due to PIK3CG deficiency — Symptoms, Testing & Specialists | Ltrl