All
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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 +
C10.228.140.163.100.050 Abetalipoproteinemia D000012 C10.228.140.163.100.320 Galactosemias D005693 C10.228.140.163.100.355 Hartnup Disease D006250 C10.228.140.163.100.360 Hepatolenticular Degeneration D006527 C10.228.140.163.100.365 Homocystinuria D006712 C10.228.140.163.100.540 Menkes Kinky Hair Syndrome D007706 C10.228.140.163.100.412 Leigh Disease D007888 C10.228.140.163.100.425 Lesch-Nyhan Syndrome D007926 C10.228.140.163.100.520 Maple Syrup Urine Disease D008375 C10.228.140.163.100.640 Oculocerebrorenal Syndrome D009800 C10.228.140.163.100.687 Phenylketonurias D010661 +
C10.228.140.163.100.725 Pyruvate Carboxylase Deficiency Disease D015324 C10.228.140.163.100.750 Pyruvate Dehydrogenase Complex Deficiency Disease D015325 C10.228.140.163.100.535 MELAS Syndrome D017241 C10.228.140.163.100.545 MERRF Syndrome D017243 C10.228.140.163.100.680 Peroxisomal Disorders D018901 +
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System D020140 +
C10.228.140.163.100.375 Hyperglycinemia, Nonketotic D020158 C10.228.140.163.100.175 Citrullinemia D020159 C10.228.140.163.100.370 Hyperargininemia D020162 C10.228.140.163.100.650 Ornithine Carbamoyltransferase Deficiency Disease D020163 C10.228.140.163.100.162 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165 C10.228.140.163.100.380 Hyperlysinemias D020167 C10.228.140.163.100.875 Tyrosinemias D020176 C10.228.140.163.100.168 Cerebral Amyloid Angiopathy, Familial D028243 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 +
C16.320.565.150.050 Abetalipoproteinemia D000012 C16.320.565.150.320 Galactosemias D005693 C16.320.565.150.355 Hartnup Disease D006250 C16.320.565.150.360 Hepatolenticular Degeneration D006527 C16.320.565.150.365 Homocystinuria D006712 C16.320.565.150.540 Menkes Kinky Hair Syndrome D007706 C16.320.565.150.412 Leigh Disease D007888 C16.320.565.150.425 Lesch-Nyhan Syndrome D007926 C16.320.565.150.520 Maple Syrup Urine Disease D008375 C16.320.565.150.640 Oculocerebrorenal Syndrome D009800 C16.320.565.150.687 Phenylketonurias D010661 +
C16.320.565.150.725 Pyruvate Carboxylase Deficiency Disease D015324 C16.320.565.150.750 Pyruvate Dehydrogenase Complex Deficiency Disease D015325 C16.320.565.150.535 MELAS Syndrome D017241 C16.320.565.150.545 MERRF Syndrome D017243 C16.320.565.150.680 Peroxisomal Disorders D018901 +
C16.320.565.150.435 Lysosomal Storage Diseases, Nervous System D020140 +
C16.320.565.150.375 Hyperglycinemia, Nonketotic D020158 C16.320.565.150.175 Citrullinemia D020159 C16.320.565.150.370 Hyperargininemia D020162 C16.320.565.150.650 Ornithine Carbamoyltransferase Deficiency Disease D020163 C16.320.565.150.162 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165 C16.320.565.150.380 Hyperlysinemias D020167 C16.320.565.150.875 Tyrosinemias D020176 C16.320.565.150.168 Cerebral Amyloid Angiopathy, Familial D028243 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 +
C18.452.100.100.050 Abetalipoproteinemia D000012 C18.452.100.100.320 Galactosemias D005693 C18.452.100.100.355 Hartnup Disease D006250 C18.452.100.100.360 Hepatolenticular Degeneration D006527 C18.452.100.100.365 Homocystinuria D006712 C18.452.100.100.540 Menkes Kinky Hair Syndrome D007706 C18.452.100.100.412 Leigh Disease D007888 C18.452.100.100.425 Lesch-Nyhan Syndrome D007926 C18.452.100.100.520 Maple Syrup Urine Disease D008375 C18.452.100.100.640 Oculocerebrorenal Syndrome D009800 C18.452.100.100.687 Phenylketonurias D010661 +
C18.452.100.100.725 Pyruvate Carboxylase Deficiency Disease D015324 C18.452.100.100.750 Pyruvate Dehydrogenase Complex Deficiency Disease D015325 C18.452.100.100.535 MELAS Syndrome D017241 C18.452.100.100.545 MERRF Syndrome D017243 C18.452.100.100.680 Peroxisomal Disorders D018901 +
C18.452.100.100.435 Lysosomal Storage Diseases, Nervous System D020140 +
C18.452.100.100.375 Hyperglycinemia, Nonketotic D020158 C18.452.100.100.175 Citrullinemia D020159 C18.452.100.100.370 Hyperargininemia D020162 C18.452.100.100.650 Ornithine Carbamoyltransferase Deficiency Disease D020163 C18.452.100.100.162 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165 C18.452.100.100.380 Hyperlysinemias D020167 C18.452.100.100.875 Tyrosinemias D020176 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 +
C18.452.648.151.050 Abetalipoproteinemia D000012 C18.452.648.151.300 Fucosidosis D005645 C18.452.648.151.320 Galactosemias D005693 C18.452.648.151.330 Glycogen Storage Disease Type II D006009 C18.452.648.151.355 Hartnup Disease D006250 C18.452.648.151.360 Hepatolenticular Degeneration D006527 C18.452.648.151.365 Homocystinuria D006712 C18.452.648.151.450 Menkes Kinky Hair Syndrome D007706 C18.452.648.151.412 Leigh Disease D007888 C18.452.648.151.425 Lesch-Nyhan Syndrome D007926 C18.452.648.151.445 Maple Syrup Urine Disease D008375 C18.452.648.151.580 Mucolipidoses D009081 C18.452.648.151.640 Oculocerebrorenal Syndrome D009800 C18.452.648.151.687 Phenylketonurias D010661 +
C18.452.648.151.825 Sphingolipidoses D013106 +
C18.452.648.151.725 Pyruvate Carboxylase Deficiency Disease D015324 C18.452.648.151.750 Pyruvate Dehydrogenase Complex Deficiency Disease D015325 C18.452.648.151.447 MELAS Syndrome D017241 C18.452.648.151.505 MERRF Syndrome D017243 C18.452.648.151.680 Peroxisomal Disorders D018901 +
C18.452.648.151.435 Lysosomal Storage Diseases, Nervous System D020140 +
C18.452.648.151.375 Hyperglycinemia, Nonketotic D020158 C18.452.648.151.175 Citrullinemia D020159 C18.452.648.151.370 Hyperargininemia D020162 C18.452.648.151.650 Ornithine Carbamoyltransferase Deficiency Disease D020163 C18.452.648.151.162 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165 C18.452.648.151.380 Hyperlysinemias D020167 C18.452.648.151.875 Tyrosinemias D020176 C18.452.648.151.168 Cerebral Amyloid Angiopathy, Familial D028243 
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