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  1. Wiskott-Aldrich syndrome: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/wiskott-aldrich-syndrome
    ... gov Catalog of Genes and Diseases from OMIM WISKOTT-ALDRICH SYNDROME; WAS Scientific Articles on PubMed PubMed References Blundell MP, Worth A, Bouma G, Thrasher AJ. ...
  2. WAS-Related Disorders - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1178
    ... Genetics Mutation Database (WAS) WASbase: Mutation registry for Wiskott-Aldrich syndrome (WAS) WAS WAS Data are compiled from the following standard references: gene from HGNC ; chromosome locus from OMIM ; protein ...
  3. Bleeding Disorder | MedlinePlus 
    https://medlineplus.gov/bleedingdisorders.html
    ... radius syndrome: MedlinePlus Genetics (National Library of Medicine) ... (National Institutes of Health) Journal Articles References and abstracts from MEDLINE/PubMed (National Library of ...
  4. WAS gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/was
    ... WAS Gene and Variant Databases NCBI Gene ... mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia. Blood. 2006 Oct ...
  5. X-linked thrombocytopenia: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/x-linked-thrombocytopenia
    ... severe disorder with similar signs and symptoms called Wiskott-Aldrich syndrome . Some people have a mild form of the ... Fillat C. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia. ...
  6. Appendices - Intrapartum care for women with existing medical conditions or obstetric complications and their babies - .... 
    https://www.ncbi.nlm.nih.gov/books/NBK546801
    ... von Willebrand Disease? or Waterhouse-Friderichsen Syndrome or Wiskott-Aldrich Syndrome or (Fibrinogen adj3 Deficien$) or Dysfibrinogenemia or Hypofibrinogenemia). ...
  7. 2019New_Mesh_Tree_Hierarchy.txt 
    https://www.nlm.nih.gov/.../download/2019New_Mesh_Tree_Hierarchy.txt
    ... Disease, Type 3 C15.378.100.100.970 Wiskott-Aldrich Syndrome C15.378.100.141 Coagulation Protein Disorders C15. ... 950 Waterhouse-Friderichsen Syndrome C15.378.463.960 Wiskott-Aldrich Syndrome C15.378.553 Leukocyte Disorders C15.378.553. ...
  8. pdf2016MeshTree.pdf 
    https://www.nlm.nih.gov/mesh/2016/download/2016MeshTree.pdf
    ... Disease, Type 3 C15.378.100.100.970...........................................Wiskott-Aldrich Syndrome C15.378.100.141...........................................Coagulation Protein Disorders C15. ...
  9. pdf2017MeshTreesWithChangesShown.pdf 
    https://www.nlm.nih.gov/.../2017MeshTreesWithChangesShown.pdf
    ... Disease, Type 2 von Willebrand Disease, Type 3 Wiskott-Aldrich Syndrome Coagulation Protein Disorders Activated Protein C Resistance Afibrinogenemia ... von Willebrand Disease, Type 3 Waterhouse-Friderichsen Syndrome Wiskott-Aldrich ... Eosinophilia Angiolymphoid Hyperplasia with Eosinophilia Eosinophilia- ...
  10. Treatment - Atopic Eczema in Children - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK49373
    ... rare diseases such as Job syndrome, Netherton syndrome, Wiskott–Aldrich syndrome, and selective IgA deficiency. Increased infection rates are ... been an undetected immune deficiency state such as Wiskott–Aldrich syndrome or a secondary bacterial infection with S. aureus ...
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