Severe Combined Immunodeficiency D016511

Related MeSH Hierarchy (4)

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

Subtype Terms (1)

X-Linked Combined Immunodeficiency Diseases
20 drugs (10 approved, 10 experimental)



Organization Involved with Other Experimental Indications (2)

Hierarchy Tree View

UMLS Data


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