Medical College of Wisconsin
CTSICores SearchResearch InformaticsREDCap

Mesh term Wiskott-Aldrich Syndrome

Browse to parent terms:
Blood Coagulation Disorders, Inherited
Genetic Diseases, X-Linked
Hemorrhagic Disorders


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.

Search for this term in our Faculty Database

View this term at the NCBI website