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Summary Literature (0)
DOID:0111987 - immunodeficiency 13

Disease Ontology Definition:A T cell deficiency characterized by decreased CD4 T-lymphocyte counts that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11.2.

Synonyms: ICL, IMD13, idiopathic CD4 lymphopenia,

Xenbase Genes : unc119



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): T cell deficiency (is_a), autosomal dominant disease (is_a)