Related MeSH Hierarchy (4)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked » X-Linked Combined Immunodeficiency Diseases
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Primary Immunodeficiency Diseases » Severe Combined Immunodeficiency » X-Linked Combined Immunodeficiency Diseases
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Infant, Newborn, Diseases » Severe Combined Immunodeficiency » X-Linked Combined Immunodeficiency Diseases
Diseases [C] » Immune System Diseases [C20] » Immunologic Deficiency Syndromes » Primary Immunodeficiency Diseases » Severe Combined Immunodeficiency » X-Linked Combined Immunodeficiency Diseases
Description
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. MeSH
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Phase 3 Indicated Drugs (1)
Phase 2 Indicated Drugs (4)
Phase 1 Indicated Drugs (3)
Organization Involved with Phase 2 Indications (9)
Organization Involved with Phase 1 Indications (2)
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