MeSH Browser

MeSH Heading: Hyperglycinemia, Nonketotic
Tree Number(s): C10.228.140.163.100.375; C16.320.565.100.477; C16.320.565.189.375; C18.452.132.100.375; C18.452.648.100.477; C18.452.648.189.375
Unique ID: D020158
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D020158
Annotation: Do not confuse with HYPERGLYCEMIC HYPEROSMOLAR NONKETOTIC COMA
Scope Note: An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system.
Entry Term(s): Glycine Encephalopathy; Hyperglycinemia, Nonketotic, Type I; Hyperglycinemia, Nonketotic, Type II; Hyperglycinemia, Nonketotic, Type III; Non-ketotic Hyperglycinemia; Nonketotic Hyperglycinemia; Nonketotic Hyperglycinemia, Type I; Nonketotic Hyperglycinemia, Type II; Nonketotic Hyperglycinemia, Type III; Type I Nonketotic Hyperglycinemia; Type II Nonketotic Hyperglycinemia; Type III Nonketotic Hyperglycinemia
Previous Indexing: Amino Acid Metabolism, Inborn Errors (1966-1998)
Public MeSH Note: 2000
History Note: 2000
Date Established: 2000/01/01
Date of Entry: 1999/11/03
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

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]
        
        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]
        
        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]
        
        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]
        
        Zellweger Syndrome [C10.228.140.163.100.968]

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]

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]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Brain Diseases, Metabolic [C18.452.132]
    - Brain Diseases, Metabolic, Inborn [C18.452.132.100]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - Amino Acid Metabolism, Inborn Errors [C18.452.648.100]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - Brain Diseases, Metabolic, Inborn [C18.452.648.189]

Hyperglycinemia, Nonketotic Preferred

Concept UI: M0328332
Scope Note: An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system.
Terms: Hyperglycinemia, Nonketotic Preferred Term
Term UI T358332
Date10/12/1999
LexicalTag NON
ThesaurusID; Nonketotic Hyperglycinemia
Term UI T368490
Date10/12/1999
LexicalTag NON
ThesaurusID; Glycine Encephalopathy
Term UI T781472
Date12/01/2010
LexicalTag NON
ThesaurusID; Non-ketotic Hyperglycinemia
Term UI T768041
Date03/26/2010
LexicalTag NON
ThesaurusID

Hyperglycinemia, Nonketotic, Type III Narrower

Hyperglycinemia, Nonketotic, Type I Narrower

Hyperglycinemia, Nonketotic, Type II Narrower

Hyperglycinemia, Nonketotic MeSH Descriptor Data 2024