Wiskott-Aldrich Syndrome (WAS)

Alias:
Eczema-Thrombocytopenia-Immunodeficiency Syndrome
Was
Immunodeficiency 2
Imd2
Wiskott-Aldrich Syndrome 1
Aldrich Syndrome
Wiskott Syndrome
Was1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Wiskott-Aldrich Syndrome, also known as eczema-thrombocytopenia-immunodeficiency syndrome, is related to immune deficiency disease and neutropenia, severe congenital, x-linked, 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 Infectious disease. The drugs gamma-Globulins and Immunoglobulin G have been mentioned in the context of this disorder. Affiliated tissues include skin and bone marrow, and related phenotypes are chronic otitis media and recurrent respiratory infections
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
AD
AR
XL
Newborn
<1/1000000
51
430
177

Medical Symptom

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Description
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No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
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References Literature

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