: MeSH: X-Linked Combined Immunodeficiency Diseases

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Primary Immunodeficiency Diseases > Severe Combined Immunodeficiency > X-Linked Combined Immunodeficiency Diseases

Immune System Diseases > Immunologic Deficiency Syndromes > Primary Immunodeficiency Diseases > Severe Combined Immunodeficiency > X-Linked Combined Immunodeficiency Diseases

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Severe Combined Immunodeficiency > X-Linked Combined Immunodeficiency Diseases

Nutritional and Metabolic Diseases > Metabolic Diseases > DNA Repair-Deficiency Disorders > Severe Combined Immunodeficiency > X-Linked Combined Immunodeficiency Diseases

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > X-Linked Combined Immunodeficiency Diseases

X-Linked Combined Immunodeficiency Diseases

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.

Combined Immunodeficiency, X-Linked
Immunodeficiency 4
Immunodeficiency 6
Immunodeficiency Diseases, X-Linked Combined
SCIDX
SCIDX1
SCID, X-Linked
Severe Combined Immunodeficiency, X-Linked
Severe Combined Immunodeficiency, X-Linked, T Cell Negative, B Cell Positive, NK Cell Negative
Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, NK Cell-Negative
X-Linked Combined Immunodeficiency
X-Linked Immunodeficiency Disease
X-Linked Immunodeficiency Syndrome
X-Linked SCID
X-Linked Severe Combined Immunodeficiency
X-SCID
XSCID

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