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 / Biomarkers
G7454 | G7456 | G196 | G3579 | G3251 | G3559 | G7852
Other Diseases
Withdrawal Syndrome | Wolcott-Rallison Syndrome | Wolff-Parkinson-White Syndrome | Wolfram Syndrome | Wolfram Syndrome 2 | Wolman Disease | Woodhouse-Sakati Syndrome | X-linked Acrogigantism | X-linked Charcot-Marie-Tooth Disease | X-linked Creatine Transporter Deficiency | X-linked Myotubular Myopathy | X-linked Sideroblastic Anemia | Xeroderma Pigmentosum | Xeroderma Pigmentosum Variant Type | Yellow Fever | Zellweger Syndrome | Zimmermann-Laband Syndrome | Zollinger-Ellison Syndrome | Zygomycosis
