About: Wiskott-Aldrich Syndrome     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • Wiskott-Aldrich Syndrome
equivalentClass
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Wiskott-Aldrich Syndrome
UMLS_CUI
  • C0043194
ALT_DEFINITION
  • A rare, X-linked immunodeficiency syndrome characterized by eczema, thrombocytopenic purpura, 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.MSH2003_2003_05_12
  • An inherited immune disorder that occurs in young boys. It causes eczema (a type of skin inflammation), a decrease in the number of platelets (blood cells that help prevent bleeding), and frequent bacterial infections. People with Wiskott-Aldrich syndrome are at increased risk of developing leukemia and lymphoma.NCI-GLOSS
Legacy_Concept_Name
  • Wiskott-Aldrich_Syndrome
FULL_SYN
  • Wiskott-Aldrich syndromePTNCI-GLOSSCDR0000539110
  • Wiskott-Aldrich SyndromePTNCI
  • Aldrich syndromePTNCI-GLOSSCDR0000562657
DEFINITION
  • A rare, X-linked immunodeficiency syndrome characterized by eczema, thrombocytopenia, and recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IgM levels are low and IgA and IgE levels are elevated. Lymphoreticular malignancies are common.NCI
code
  • C3448
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