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Human Disease

CD3epsilon deficiency

Term ID
DOID:0060017
Synonyms
Definition
A severe combined immunodeficiency that has_material_basis_in autosomal recessive mutations in the gene coding for T-cell surface glycoprotein CD3epsilon chain precursors. Patients with CD3epsilon deficiency have a severe defect in the expression of the T-cell receptor CD3-complex. https://www.ncbi.nlm.nih.gov/pubmed/16264327
References
Ontology
Human Disease   ( DOID:0060017 )
Relationships
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Genes Involved
Zebrafish Models