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982 results
  1. 2019New_Mesh_Tree_Hierarchy.txt 
    https://www.nlm.nih.gov/.../download/2019New_Mesh_Tree_Hierarchy.txt
    ... 435.825.300.300.750 Tay-Sachs Disease, AB Variant C10.228.140.163.100.435.825.300. ... 435.825.300.300.750 Tay-Sachs Disease, AB Variant C16.320.565.189.435.825.300.400 ...
  2. pdf2017MeshTreesWithChangesShown.pdf 
    https://www.nlm.nih.gov/.../2017MeshTreesWithChangesShown.pdf
    ... Sandhoff Disease Tay-Sachs Disease Tay-Sachs Disease, AB Variant Gangliosidosis, GM1 Gaucher Disease Leukodystrophy, Globoid Cell Niemann- ... Sandhoff Disease Tay-Sachs Disease Tay-Sachs Disease, AB Variant Gangliosidosis, GM1 Gaucher Disease Leukodystrophy, Globoid Cell Niemann- ...
  3. pdf2016MeshTree.pdf 
    https://www.nlm.nih.gov/mesh/2016/download/2016MeshTree.pdf
    ... 435.825.300.300.750...........................................Tay-Sachs Disease, AB Variant C10.228.140.163.100.435.825.300. ... 435.825.300.300.750...........................................Tay-Sachs Disease, AB Variant C16.320.565.189.435.825.300.400........................................... ...
  4. GM2 activator deficiency: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/gm2-activator-deficiency
    ... Description GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant) is a rare inherited disorder that causes progressive ... condition. Other Names for This Condition GM2 gangliosidosis, AB variant Hexosaminidase activator deficiency Tay-Sachs disease, AB variant ...
  5. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... p >GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant) is a rare inherited disorder that causes progressive ... related-gene-list><synonym-list ><synonym >GM2 gangliosidosis, AB variant</synonym><synonym >Hexosaminidase activator deficiency</synonym><synonym >Tay- ...
  6. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... deficiency</title><other_names ><other_name >GM2 gangliosidosis, AB variant</other_name><other_name >Hexosaminidase activator deficiency</other_ ...
  7. GM2A gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/gm2a
    ... with GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant). This is a rare inherited disorder that results ... activator deficiency in two patients with GM2-gangliosidosis AB variant. Am J Hum Genet. 1996 Nov;59(5): ...
  8. Degenerative Nerve Diseases 
    https://medlineplus.gov/degenerativenervediseases.html
    Neurodegenerative (degenerative nerve) diseases are disorders that destroy motor neurons. Parkinson's is an examples. See a list of all the diseases. ... Degenerative nerve ...
  9. Hereditary Dystonia Overview - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1155
    ... hypomyelination on T 2 -weighted images GM2-gangliosidosis, AB variant AR GM2A Indistinguishable from GM1-gangliosidosis Leukodystrophies Creatine ...
  10. Genetic Conditions: G 
    https://medlineplus.gov/genetics/condition-g
    ... Aspartylglucosaminuria GM1 gangliosidosis GM2 activator deficiency GM2 gangliosidosis, AB variant, see GM2 activator deficiency GM2 gangliosidosis, type 1, ...
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