Diehtu doahpagis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Ávžžuhuvvon tearbma
Wiskott-Aldrich Syndrome
Tiipa
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Topical Descriptor
Badjedoaba
Stivrentearpmat
- Aldrich Syndrome
- Eczema Thrombocytopenia Immunodeficiency Syndrome
- Eczema-Thrombocytopenia-Immunodeficiency Syndrome
- Eczema-Thrombocytopenia-Immunodeficiency Syndromes
- Imd2
- Immunodeficiency 2
- Immunodeficiency 2s
- Wiskott Syndrome
- Wiskott Syndromes
Fuomášahttin
- 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.
Fuomášahttin rievdadanhistorjjás
- 85; was ALDRICH SYNDROME 1963-84
Eará gielain
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Finnish
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Aldrich
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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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