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50 results
  1. ... disorders. Learn more about the gene associated with Wiskott-Aldrich syndrome WAS Inheritance This condition is inherited in an ...
  2. ... life [score of 5]) [ Albert et al 2010 ]. Wiskott-Aldrich Syndrome Wiskott-Aldrich syndrome usually presents in infancy. Although ... with germline pathogenic variants in WAS . Differential Diagnosis Wiskott-Aldrich Syndrome Idiopathic thrombocytopenic purpura (ITP ) should be considered in ...
  3. ... immune synapse). Health Conditions Related to Genetic Changes Wiskott-Aldrich syndrome More than 350 mutations in the WAS gene have been found to cause Wiskott-Aldrich syndrome, a condition characterized by abnormal immune system function ( ...
  4. ... published></health-condition-summary><health-condition-summary ><name >Wiskott-Aldrich syndrome</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
  5. ... 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. ... 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. ...
  7. ... 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- ...
  8. ... Disease, Type 3 C15.378.100.100.970...........................................Wiskott-Aldrich Syndrome C15.378.100.141...........................................Coagulation Protein Disorders C15. ...
  9. ... von Willebrand Disease? or Waterhouse-Friderichsen Syndrome or Wiskott-Aldrich Syndrome or (Fibrinogen adj3 Deficien$) or Dysfibrinogenemia or Hypofibrinogenemia). ...
  10. ... congenital alopecia, and nail dystrophy Wiskott syndrome, see Wiskott-Aldrich syndrome Wiskott-Aldrich syndrome WM, see Waldenström macroglobulinemia WMS, ...
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