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Summary Literature (0)
DOID:0060018 - CD3gamma deficiency


Disease Ontology Definition:A severe combined immunodeficiency that has_material_basis_in autosomal recessive mutations in the gene coding for T-cell surface glycoprotein CD3gamma chain precursors. Patients with CD3gamma deficiency have a severe defect in the expression of the T-cell receptor CD3-complex. Affected patients have decreased T-cell numbers and function; B cells are variably affected.

Synonyms:

Xenbase Genes : cd3g

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014276 - combined immunodeficiency due to CD3gamma deficiency


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), severe combined immunodeficiency (is_a)