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.