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C10 Nervous System Diseases D009422 +
C10.228 Central Nervous System Diseases D002493 +
C10.228.140 Brain Diseases D001927 +
C10.228.140.163 Brain Diseases, Metabolic D001928 +
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn D020739 +
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System D020140 +
C10.228.140.163.100.435.825 Sphingolipidoses D013106 +
C10.228.140.163.100.435.825.200 Fabry Disease D000795
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
C16.320 Genetic Diseases, Inborn D030342 +
C16.320.322 Genetic Diseases, X-Linked D040181 +
C16.320.322.124 Fabry Disease D000795
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
C16.320 Genetic Diseases, Inborn D030342 +
C16.320.565 Metabolism, Inborn Errors D008661 +
C16.320.565.150 Brain Diseases, Metabolic, Inborn D020739 +
C16.320.565.150.435 Lysosomal Storage Diseases, Nervous System D020140 +
C16.320.565.150.435.825 Sphingolipidoses D013106 +
C16.320.565.150.435.825.200 Fabry Disease D000795
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
C16.320 Genetic Diseases, Inborn D030342 +
C16.320.565 Metabolism, Inborn Errors D008661 +
C16.320.565.556 Lipid Metabolism, Inborn Errors D008052 +
C16.320.565.556.641 Lipoidosis D008064 +
C16.320.565.556.641.803 Sphingolipidoses D013106 +
C16.320.565.556.641.803.300 Fabry Disease D000795
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
C16.320 Genetic Diseases, Inborn D030342 +
C16.320.565 Metabolism, Inborn Errors D008661 +
C16.320.565.580 Lysosomal Storage Diseases D016464 +
C16.320.565.580.554 Lysosomal Storage Diseases, Nervous System D020140 +
C16.320.565.580.554.825 Sphingolipidoses D013106 +
C16.320.565.580.554.825.200 Fabry Disease D000795
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
C16.320 Genetic Diseases, Inborn D030342 +
C16.320.565 Metabolism, Inborn Errors D008661 +
C16.320.565.580 Lysosomal Storage Diseases D016464 +
C16.320.565.580.803 Sphingolipidoses D013106 +
C16.320.565.580.803.300 Fabry Disease D000795
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.100 Brain Diseases, Metabolic D001928 +
C18.452.100.100 Brain Diseases, Metabolic, Inborn D020739 +
C18.452.100.100.435 Lysosomal Storage Diseases, Nervous System D020140 +
C18.452.100.100.435.825 Sphingolipidoses D013106 +
C18.452.100.100.435.825.200 Fabry Disease D000795
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.648 Metabolism, Inborn Errors D008661 +
C18.452.648.151 Brain Diseases, Metabolic, Inborn D020739 +
C18.452.648.151.435 Lysosomal Storage Diseases, Nervous System D020140 +
C18.452.648.151.435.825 Sphingolipidoses D013106 +
C18.452.648.151.435.825.200 Fabry Disease D000795
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.648 Metabolism, Inborn Errors D008661 +
C18.452.648.151 Brain Diseases, Metabolic, Inborn D020739 +
C18.452.648.151.825 Sphingolipidoses D013106 +
C18.452.648.151.825.200 Fabry Disease D000795
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.648 Metabolism, Inborn Errors D008661 +
C18.452.648.556 Lipid Metabolism, Inborn Errors D008052 +
C18.452.648.556.641 Lipoidosis D008064 +
C18.452.648.556.641.803 Sphingolipidoses D013106 +
C18.452.648.556.641.803.300 Fabry Disease D000795
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.648 Metabolism, Inborn Errors D008661 +
C18.452.648.595 Lysosomal Storage Diseases D016464 +
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System D020140 +
C18.452.648.595.554.825 Sphingolipidoses D013106 +
C18.452.648.595.554.825.200 Fabry Disease D000795
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.648 Metabolism, Inborn Errors D008661 +
C18.452.648.595 Lysosomal Storage Diseases D016464 +
C18.452.648.595.803 Sphingolipidoses D013106 +
C18.452.648.595.803.300 Fabry Disease D000795
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