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66 results
  1. ... identified. Learn more about the genes associated with Autoimmune lymphoproliferative syndrome FAS KRAS MAGT1 NRAS PIK3CD STAT3 Additional Information ...
  2. ... not needed. Health Conditions Related to Genetic Changes Autoimmune lymphoproliferative syndrome At least 115 mutations in the FAS gene ... with a disorder of the immune system called autoimmune lymphoproliferative syndrome (ALPS). ALPS is characterized by the production of ...
  3. ... about Noonan syndrome More About This Health Condition Autoimmune lymphoproliferative syndrome MedlinePlus Genetics provides information about Autoimmune lymphoproliferative syndrome ...
  4. ... about Noonan syndrome More About This Health Condition Autoimmune lymphoproliferative syndrome MedlinePlus Genetics provides information about Autoimmune lymphoproliferative syndrome ...
  5. ... cancer called lymphoma. More About This Health Condition Autoimmune lymphoproliferative syndrome MedlinePlus Genetics provides information about Autoimmune lymphoproliferative syndrome ...
  6. ... in AD-HIES. More About This Health Condition Autoimmune lymphoproliferative syndrome MedlinePlus Genetics provides information about Autoimmune lymphoproliferative syndrome ...
  7. ... infection and illness. More About This Health Condition Autoimmune lymphoproliferative syndrome MedlinePlus Genetics provides information about Autoimmune lymphoproliferative syndrome ...
  8. ... published></health-condition-summary><health-condition-summary ><name >Autoimmune lymphoproliferative syndrome</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
  9. ... Filarial Non-Filarial Lymphedema Lymphocele Lymphoproliferative Disorders Agammaglobulinemia Autoimmune Lymphoproliferative Syndrome Giant Lymph Node Hyperplasia Granuloma Angiolymphoid Hyperplasia with ...
  10. ... 604.515.032 Agammaglobulinemia C15.604.515.138 Autoimmune Lymphoproliferative Syndrome C15.604.515.245 Castleman Disease C15.604. ... C16.320.080 Ataxia Telangiectasia C16.320.089 Autoimmune Lymphoproliferative Syndrome C16.320.099 Blood Coagulation Disorders, Inherited C16. ...
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