Related MeSH Hierarchy (4)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Primary Immunodeficiency Diseases » Severe Combined Immunodeficiency
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Infant, Newborn, Diseases » Severe Combined Immunodeficiency
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » DNA Repair-Deficiency Disorders » Severe Combined Immunodeficiency
Diseases [C] » Immune System Diseases [C20] » Immunologic Deficiency Syndromes » Primary Immunodeficiency Diseases » Severe Combined Immunodeficiency
Description
Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). MeSH
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Subtype Terms (1)
X-Linked Combined Immunodeficiency Diseases
20 drugs (10 approved, 10 experimental)
Approved Indicated Drugs (2)
Phase 3 Indicated Drugs (3)
Phase 2 Indicated Drugs (12)
Phase 1 Indicated Drugs (6)
Other Experimental Indicated Drugs (4)
Organization Involved with Phase 3 Indications (6)
Organization Involved with Phase 2 Indications (24)
Assistance Publique - Hôpitaux de Paris
California Institute for Regenerative Medicine
Organization Involved with Phase 1 Indications (5)
Organization Involved with Other Experimental Indications (2)
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UMLS Data
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