Definition: Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified.
Other names X-Linked Immunodeficiency Syndromes; X-Linked Immunodeficiency Diseases; X-Linked Combined Immunodeficiencies; X Linked Severe Combined Immunodeficiency; X Linked Immunodeficiency Syndrome; X Linked Immunodeficiency Disease; X Linked Combined Immunodeficiency Diseases; X Linked Combined Immunodeficiency; Syndromes, X-Linked Immunodeficiency; Immunodeficiency, X-Linked Combined; Immunodeficiency Syndromes, X-Linked; Immunodeficiency Syndrome, X-Linked; Immunodeficiency Diseases, X-Linked; Immunodeficiency Diseases, X Linked Combined; Immunodeficiency Disease, X-Linked; Combined Immunodeficiency, X-Linked; Combined Immunodeficiencies, X-Linked; X-Linked Immunodeficiency Syndrome; X-Linked Immunodeficiency Disease; X-Linked Combined Immunodeficiency
