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Familial CD8 deficiency

disorder
SNOMED 766983005CUI C1837065

Overview

Familial CD8 deficiency is a disorder.

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Absence of CD8-positive T cells
HP:0005422
Bronchiectasis
HP:0002110
Recurrent bacterial infections
HP:0002718
Recurrent viral infections
HP:0004429
respiratory infections, recurrent
HP:0002205

Quick Facts

SNOMED CT
766983005
UMLS CUI
C1837065
Fully Specified Name
Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
5
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.