Related MeSH Hierarchy (8)
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Hemorrhagic Disorders » Wiskott-Aldrich Syndrome
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Leukocyte Disorders » Leukopenia » Lymphopenia » Wiskott-Aldrich Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Blood Coagulation Disorders, Inherited » Wiskott-Aldrich Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked » Wiskott-Aldrich Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Primary Immunodeficiency Diseases » Wiskott-Aldrich Syndrome
Diseases [C] » Immune System Diseases [C20] » Immunologic Deficiency Syndromes » Lymphopenia » Wiskott-Aldrich Syndrome
Diseases [C] » Immune System Diseases [C20] » Immunologic Deficiency Syndromes » Primary Immunodeficiency Diseases » Wiskott-Aldrich Syndrome
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Coagulation Disorders » Blood Coagulation Disorders, Inherited » Wiskott-Aldrich Syndrome
Description
A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common. MeSH
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Phase 4 Indicated Drugs (1)
Phase 3 Indicated Drugs (1)
Phase 1 Indicated Drugs (3)
Other Experimental Indicated Drugs (6)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (3)
Organization Involved with Phase 2 Indications (20)
Organization Involved with Phase 1 Indications (4)
Organization Involved with Other Experimental Indications (1)
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