Wiskott-Aldrich Syndrome

About the Disease
Wiskott-Aldrich Syndrome, also known as eczema-thrombocytopenia-immunodeficiency syndrome, is related to neutropenia, severe congenital, x-linked and spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2, and has symptoms including diarrhea and petechiae of skin. An important gene associated with Wiskott-Aldrich Syndrome is WAS (WASP Actin Nucleation Promoting Factor), and among its related pathways/superpathways are Innate Immune System and Disease. The drugs gamma-Globulins and Antibodies have been mentioned in the context of this disorder. Affiliated tissues include skin, bone marrow and t cells, and related phenotypes are chronic otitis media and recurrent respiratory infections

Common Targets
WAS | WIPF1 | G196 | CXCR2 | HPRT1 | IL2RA | G7852

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