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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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