Autosomal recessive combined immunodeficiency due to IL6 receptor protein deficiency

disorder

SNOMED 1351327002CUI C5925112

Overview

Autosomal recessive combined immunodeficiency due to IL6 receptor protein deficiency is a disorder.

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

Related Conditions

Hyperimmunoglobulin E syndrome(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1351327002
UMLS CUI: C5925112
Fully Specified Name: Autosomal recessive combined immunodeficiency due to interleukin 6 receptor 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.