T-cell immunodeficiency due to RHOH (ras homolog family member H) deficiency

disorder

SNOMED 770785002CUI C4749500

Overview

T-cell immunodeficiency due to RHOH (ras homolog family member H) deficiency is a disorder.

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Primary immune deficiency disorder(parent)

Quick Facts

SNOMED CT: 770785002
UMLS CUI: C4749500
Fully Specified Name: T-cell immunodeficiency due to ras homolog family member H 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.