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Autosomal recessive agammaglobulinemia due to solute carrier family 39 member 7 deficiency

disorder
SNOMED 1351665003CUI C5968874

Overview

Autosomal recessive agammaglobulinemia due to solute carrier family 39 member 7 deficiency is a disorder.

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

Related Conditions

Autosomal recessive agammaglobulinemia(parent)

Quick Facts

SNOMED CT
1351665003
UMLS CUI
C5968874
Fully Specified Name
Autosomal recessive agammaglobulinemia due to solute carrier family 39 member 7 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.