Hyperglycinemia, Nonketotic

进入的组:

Hyperglycinemias, Nonketotic
Nonketotic Hyperglycinemias
Nonketotic Hyperglycinemia
Glycine Encephalopathy
Encephalopathies, Glycine
Encephalopathy, Glycine
Glycine Encephalopathies
Non-ketotic Hyperglycinemia
Hyperglycinemia, Non-ketotic
Hyperglycinemias, Non-ketotic
Non ketotic Hyperglycinemia
Non-ketotic Hyperglycinemias
Hyperglycinemia, Nonketotic, Type III
Type III Nonketotic Hyperglycinemia
Nonketotic Hyperglycinemia, Type III
Hyperglycinemia, Nonketotic, Type I
Type I Nonketotic Hyperglycinemia
Nonketotic Hyperglycinemia, Type I
Hyperglycinemia, Nonketotic, Type II
Type II Nonketotic Hyperglycinemia
Nonketotic Hyperglycinemia, Type II

All MeSH Categories
- Diseases Category
  - Nervous System Diseases [C10]
    - Central Nervous System Diseases [C10.228]
      - Brain Diseases [C10.228.140]
        
        Brain Diseases, Metabolic [C10.228.140.163]
        
        Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
        
        Adrenoleukodystrophy [C10.228.140.163.100.084]
        
        Cerebral Amyloid Angiopathy, Familial [C10.228.140.163.100.168]
        
        Galactosemias [C10.228.140.163.100.320]
        
        Hartnup Disease [C10.228.140.163.100.355]
        
        Hepatolenticular Degeneration [C10.228.140.163.100.360]
        
        Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.163.100.362] add_circle
        
        Homocystinuria [C10.228.140.163.100.365]
        
        Hyperglycinemia, Nonketotic [C10.228.140.163.100.375]
        
        Hyperlysinemias [C10.228.140.163.100.380]
        
        Leigh Disease [C10.228.140.163.100.412]
        
        Lesch-Nyhan Syndrome [C10.228.140.163.100.425]
        
        Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435] add_circle
        
        Maple Syrup Urine Disease [C10.228.140.163.100.520]
        
        MELAS Syndrome [C10.228.140.163.100.535]
        
        Menkes Kinky Hair Syndrome [C10.228.140.163.100.540]
        
        MERRF Syndrome [C10.228.140.163.100.545]
        
        Mevalonate Kinase Deficiency [C10.228.140.163.100.593]
        
        Oculocerebrorenal Syndrome [C10.228.140.163.100.640]
        
        Phenylketonurias [C10.228.140.163.100.687] add_circle
        
        Pyruvate Carboxylase Deficiency Disease [C10.228.140.163.100.725]
        
        Pyruvate Dehydrogenase Complex Deficiency Disease [C10.228.140.163.100.750]
        
        Refsum Disease [C10.228.140.163.100.813]
        
        Refsum Disease, Infantile [C10.228.140.163.100.844]
        
        Tyrosinemias [C10.228.140.163.100.875]
        
        Urea Cycle Disorders, Inborn [C10.228.140.163.100.937] add_circle
        
        Zellweger Syndrome [C10.228.140.163.100.968]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Metabolism, Inborn Errors [C16.320.565]
        
        Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
        
        Albinism [C16.320.565.100.102] add_circle
        
        Alkaptonuria [C16.320.565.100.187]
        
        Hyperglycinemia, Nonketotic [C16.320.565.100.477]
        
        Hyperhomocysteinemia [C16.320.565.100.480] add_circle
        
        Hyperlysinemias [C16.320.565.100.544]
        
        Maple Syrup Urine Disease [C16.320.565.100.608]
        
        Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C16.320.565.100.614]
        
        Multiple Carboxylase Deficiency [C16.320.565.100.620] add_circle
        
        Phenylketonurias [C16.320.565.100.766] add_circle
        
        Prolidase Deficiency [C16.320.565.100.794]
        
        Propionic Acidemia [C16.320.565.100.823]
        
        Tyrosinemias [C16.320.565.100.880]
        
        Urea Cycle Disorders, Inborn [C16.320.565.100.940] add_circle

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Metabolism, Inborn Errors [C16.320.565]
        
        Brain Diseases, Metabolic, Inborn [C16.320.565.189]
        
        Adrenoleukodystrophy [C16.320.565.189.084]
        
        Cerebral Amyloid Angiopathy, Familial [C16.320.565.189.168]
        
        Galactosemias [C16.320.565.189.320]
        
        Hartnup Disease [C16.320.565.189.355]
        
        Hepatolenticular Degeneration [C16.320.565.189.360]
        
        Hereditary Central Nervous System Demyelinating Diseases [C16.320.565.189.362] add_circle
        
        Homocystinuria [C16.320.565.189.365]
        
        Hyperglycinemia, Nonketotic [C16.320.565.189.375]
        
        Hyperlysinemias [C16.320.565.189.380]
        
        Leigh Disease [C16.320.565.189.412]
        
        Lesch-Nyhan Syndrome [C16.320.565.189.425]
        
        Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435] add_circle
        
        Maple Syrup Urine Disease [C16.320.565.189.520]
        
        MELAS Syndrome [C16.320.565.189.535]
        
        Menkes Kinky Hair Syndrome [C16.320.565.189.540]
        
        MERRF Syndrome [C16.320.565.189.545]
        
        Mevalonate Kinase Deficiency [C16.320.565.189.593]
        
        Oculocerebrorenal Syndrome [C16.320.565.189.640]
        
        Phenylketonurias [C16.320.565.189.687] add_circle
        
        Pyruvate Carboxylase Deficiency Disease [C16.320.565.189.725]
        
        Pyruvate Dehydrogenase Complex Deficiency Disease [C16.320.565.189.750]
        
        Refsum Disease [C16.320.565.189.813]
        
        Refsum Disease, Infantile [C16.320.565.189.844]
        
        Tyrosinemias [C16.320.565.189.875]
        
        Urea Cycle Disorders, Inborn [C16.320.565.189.937] add_circle
        
        Zellweger Syndrome [C16.320.565.189.968]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Brain Diseases, Metabolic [C18.452.132]
        
        Brain Diseases, Metabolic, Inborn [C18.452.132.100]
        
        Adrenoleukodystrophy [C18.452.132.100.084]
        
        Cerebral Amyloid Angiopathy, Familial [C18.452.132.100.168]
        
        Galactosemias [C18.452.132.100.320]
        
        Hartnup Disease [C18.452.132.100.355]
        
        Hepatolenticular Degeneration [C18.452.132.100.360]
        
        Hereditary Central Nervous System Demyelinating Diseases [C18.452.132.100.362] add_circle
        
        Homocystinuria [C18.452.132.100.365]
        
        Hyperglycinemia, Nonketotic [C18.452.132.100.375]
        
        Hyperlysinemias [C18.452.132.100.380]
        
        Leigh Disease [C18.452.132.100.412]
        
        Lesch-Nyhan Syndrome [C18.452.132.100.425]
        
        Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435] add_circle
        
        Maple Syrup Urine Disease [C18.452.132.100.520]
        
        MELAS Syndrome [C18.452.132.100.535]
        
        Menkes Kinky Hair Syndrome [C18.452.132.100.540]
        
        MERRF Syndrome [C18.452.132.100.545]
        
        Mevalonate Kinase Deficiency [C18.452.132.100.593]
        
        Oculocerebrorenal Syndrome [C18.452.132.100.640]
        
        Phenylketonurias [C18.452.132.100.687] add_circle
        
        Pyruvate Carboxylase Deficiency Disease [C18.452.132.100.725]
        
        Pyruvate Dehydrogenase Complex Deficiency Disease [C18.452.132.100.750]
        
        Refsum Disease [C18.452.132.100.813]
        
        Refsum Disease, Infantile [C18.452.132.100.844]
        
        Tyrosinemias [C18.452.132.100.875]
        
        Urea Cycle Disorders, Inborn [C18.452.132.100.937] add_circle
        
        Zellweger Syndrome [C18.452.132.100.968]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Metabolism, Inborn Errors [C18.452.648]
        
        Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
        
        Albinism [C18.452.648.100.102] add_circle
        
        Alkaptonuria [C18.452.648.100.187]
        
        Hyperglycinemia, Nonketotic [C18.452.648.100.477]
        
        Hyperhomocysteinemia [C18.452.648.100.480] add_circle
        
        Hyperlysinemias [C18.452.648.100.544]
        
        Maple Syrup Urine Disease [C18.452.648.100.608]
        
        Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C18.452.648.100.614]
        
        Multiple Carboxylase Deficiency [C18.452.648.100.620] add_circle
        
        Phenylketonurias [C18.452.648.100.766] add_circle
        
        Propionic Acidemia [C18.452.648.100.823]
        
        Tyrosinemias [C18.452.648.100.880]
        
        Urea Cycle Disorders, Inborn [C18.452.648.100.940] add_circle

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Metabolism, Inborn Errors [C18.452.648]
        
        Brain Diseases, Metabolic, Inborn [C18.452.648.189]
        
        Adrenoleukodystrophy [C18.452.648.189.084]
        
        Cerebral Amyloid Angiopathy, Familial [C18.452.648.189.168]
        
        Galactosemias [C18.452.648.189.320]
        
        Hartnup Disease [C18.452.648.189.355]
        
        Hepatolenticular Degeneration [C18.452.648.189.360]
        
        Hereditary Central Nervous System Demyelinating Diseases [C18.452.648.189.362] add_circle
        
        Homocystinuria [C18.452.648.189.365]
        
        Hyperglycinemia, Nonketotic [C18.452.648.189.375]
        
        Hyperlysinemias [C18.452.648.189.380]
        
        Leigh Disease [C18.452.648.189.412]
        
        Lesch-Nyhan Syndrome [C18.452.648.189.425]
        
        Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435] add_circle
        
        Maple Syrup Urine Disease [C18.452.648.189.520]
        
        MELAS Syndrome [C18.452.648.189.535]
        
        Menkes Kinky Hair Syndrome [C18.452.648.189.540]
        
        MERRF Syndrome [C18.452.648.189.545]
        
        Mevalonate Kinase Deficiency [C18.452.648.189.593]
        
        Oculocerebrorenal Syndrome [C18.452.648.189.640]
        
        Phenylketonurias [C18.452.648.189.687] add_circle
        
        Pyruvate Carboxylase Deficiency Disease [C18.452.648.189.725]
        
        Pyruvate Dehydrogenase Complex Deficiency Disease [C18.452.648.189.750]
        
        Refsum Disease [C18.452.648.189.813]
        
        Refsum Disease, Infantile [C18.452.648.189.844]
        
        Tyrosinemias [C18.452.648.189.875]
        
        Urea Cycle Disorders, Inborn [C18.452.648.189.937] add_circle
        
        Zellweger Syndrome [C18.452.648.189.968]

MeSH 搜索器

Hyperglycinemia, Nonketotic

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