Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
[show all 9 paths]
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Preferred term
Wiskott-Aldrich Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- Aldrich Syndrome
- Eczema Thrombocytopenia Immunodeficiency Syndrome
- Eczema-Thrombocytopenia-Immunodeficiency Syndrome
- Eczema-Thrombocytopenia-Immunodeficiency Syndromes
- Imd2
- Immunodeficiency 2
- Immunodeficiency 2s
- Wiskott Syndrome
- Wiskott Syndromes
Scope note
- 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.
History note
- 85; was ALDRICH SYNDROME 1963-84
In other languages
-
Finnish
-
Aldrich
-
deficientia immunalis cum thrombocytopenia et eczemate
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immunbrist med trombocytopeni och eksem
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immuunivajavuus ja trombosytopenia ja ekseema
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syndroma Wiskott-Aldrich
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Wiskott
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Wiskott-Aldrich
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Wiskott-Aldrichin syndrooma
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Swedish
URI
http://www.yso.fi/onto/mesh/D014923
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