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6 results
  1. ... the DTNBP1 gene are associated with Type 7 HERMANSKY-PUDLAK SYNDROME and SCHIZOPHRENIA. Tree locations: Dystrophin-Associated Proteins D12. ... an-allergy-or-intolerance. Tree locations: Signs and Symptoms, Digestive C23.888.821.387 New MeSH Headings ...
  2. ... lipid storage diseases (e.g.,LCAT DEFICIENCY; and HERMANSKY-PUDLAK SYNDROME). Tree locations: Cytoplasmic Granules A11.284.430.214. ... result in multiple and variable inflammatory and allergic symptoms. These disorders are associated with various mutations in ...
  3. ... lipid storage diseases (e.g.,LCAT DEFICIENCY; and HERMANSKY- PUDLAK SYNDROME). Memory B Cells A subset of activated B ... When persistent infections are cleared so that infection symptoms are under control they are often referred to ...
  4. ... 545 Albinism, Oculocutaneous C11.270.040.545.400 Hermanski-Pudlak Syndrome C11.270.040.772 Chediak-Higashi Syndrome C11. ... 510 Hemophilia B C15.378.100.100.515 Hermanski-Pudlak Syndrome C15.378.100.100.550 Hypoprothrombinemias C15.378. ...
  5. ... Hereditary Aicardi Syndrome Albinism Albinism, Ocular Albinism, Oculocutaneous Hermanski-Pudlak Syndrome Aniridia WAGR Syndrome Choroideremia Cone-Rod Dystrophies Corneal ...
  6. ... 545...........................................Albinism, Oculocutaneous C11.270.040.545.400...........................................Hermanski-Pudlak Syndrome C11.270.060...........................................Aniridia C11.270.060.950........................................... ...