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6 results
  1. pdf2022NewMeSHheadingsforNewYearsinglecolumnPBI.pdf 
    https://www.nlm.nih.gov/...MeSHheadingsforNewYearsinglecolumnPBI.pdf
    ... lipid storage diseases (e.g.,LCAT DEFICIENCY; and HERMANSKY-PUDLAK SYNDROME). Tree locations: Cytoplasmic Granules A11.284.430.214. ...
  2. pdf2018NewHeadingsSingleColumn508.pdf 
    https://www.nlm.nih.gov/.../2018NewHeadingsSingleColumn508.pdf
    ... the DTNBP1 gene are associated with Type 7 HERMANSKY-PUDLAK SYNDROME and SCHIZOPHRENIA. Tree locations: Dystrophin-Associated Proteins D12. ...
  3. pdf2022NewheadingsbycategorywithScopeNotes.pdf 
    https://www.nlm.nih.gov/...22NewheadingsbycategorywithScopeNotes.pdf
    ... lipid storage diseases (e.g.,LCAT DEFICIENCY; and HERMANSKY- PUDLAK SYNDROME). Memory B Cells A subset of activated B ...
  4. 2019New_Mesh_Tree_Hierarchy.txt 
    https://www.nlm.nih.gov/.../download/2019New_Mesh_Tree_Hierarchy.txt
    ... 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. pdf2016MeshTree.pdf 
    https://www.nlm.nih.gov/mesh/2016/download/2016MeshTree.pdf
    ... 545...........................................Albinism, Oculocutaneous C11.270.040.545.400...........................................Hermanski-Pudlak Syndrome C11.270.060...........................................Aniridia C11.270.060.950........................................... ...
  6. pdf2017MeshTreesWithChangesShown.pdf 
    https://www.nlm.nih.gov/.../2017MeshTreesWithChangesShown.pdf
    ... Hereditary Aicardi Syndrome Albinism Albinism, Ocular Albinism, Oculocutaneous Hermanski-Pudlak Syndrome Aniridia WAGR Syndrome Choroideremia Cone-Rod Dystrophies Corneal ...