Triple X syndrome, epilepsy, and hypogammaglobulinemia

disorder

SNOMED 234639001CUI C0472821

Overview

Triple X syndrome, epilepsy, and hypogammaglobulinemia is a disorder.

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

Related Conditions

Immunodeficiency associated with chromosomal abnormality(parent)

Disorder of immune structure(parent)

Quick Facts

SNOMED CT: 234639001
UMLS CUI: C0472821
Fully Specified Name: Triple X syndrome, epilepsy, and hypogammaglobulinemia (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.