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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, idiopathic CD4 lymphopenia, IMD13

Xenbase Genes : unc119


MIM:
MIM:615518 - IMMUNODEFICIENCY 13; IMD13

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

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