X-linked common variable immunodeficiency due to SH3KBP1 deficiency

disorder

SNOMED 1351642008CUI C5968856

Overview

X-linked common variable immunodeficiency due to SH3KBP1 deficiency is a disorder.

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

Related Conditions

X-linked recessive hereditary disease(parent)

Common variable immunodeficiency(parent)

Hereditary disorder of immune system(parent)

Quick Facts

SNOMED CT: 1351642008
UMLS CUI: C5968856
Fully Specified Name: X-linked common variable immunodeficiency due to SH3 domain containing kinase binding protein 1 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.