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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Metabolism, Inborn Errors [MESH:D008661] > Brain Diseases, Metabolic, Inborn [MESH:D020739] > Lysosomal Storage Diseases, Nervous System [MESH:D020140] > Sphingolipidoses [MESH:D013106] > Gangliosidoses [MESH:D005733] > Gangliosidoses, GM2 [MESH:D020143] > Sandhoff Disease [MESH:D012497] |
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C11. Eye Diseases: Z. Exceptions |
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Metabolism, Inborn Errors [MESH:D008661] > Brain Diseases, Metabolic, Inborn [MESH:D020739] > Lysosomal Storage Diseases, Nervous System [MESH:D020140] > Sphingolipidoses [MESH:D013106] > Gangliosidoses [MESH:D005733] > Gangliosidoses, GM2 [MESH:D020143] > Sandhoff Disease [MESH:D012497] |
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