Hyperglycinemia, Nonketotic
"Hyperglycinemia, Nonketotic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system.
MeSH 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
Concept/Terms
Hyperglycinemia, Nonketotic- Hyperglycinemia, Nonketotic
- 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
Below are MeSH descriptors whose meaning is more general than "Hyperglycinemia, Nonketotic".
- Diseases [C]
- 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]
- Hyperglycinemia, Nonketotic [C10.228.140.163.100.375]
- 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]
- Hyperglycinemia, Nonketotic [C16.320.565.100.477]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Hyperglycinemia, Nonketotic [C16.320.565.189.375]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Hyperglycinemia, Nonketotic [C18.452.132.100.375]
- Metabolism, Inborn Errors [C18.452.648]
- Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
- Hyperglycinemia, Nonketotic [C18.452.648.100.477]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Hyperglycinemia, Nonketotic [C18.452.648.189.375]
Below are MeSH descriptors whose meaning is more specific than "Hyperglycinemia, Nonketotic".
This graph shows the total number of publications written about "Hyperglycinemia, Nonketotic" by people in Harvard Catalyst Profiles by year, and whether "Hyperglycinemia, Nonketotic" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2003 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
Below are the most recent publications written about "Hyperglycinemia, Nonketotic" by people in Profiles.
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Ketogenic diet as a glycine lowering therapy in nonketotic hyperglycinemia and impact on brain glycine levels. Orphanet J Rare Dis. 2022 12 05; 17(1):423.
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Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans. Hum Genet. 2016 Nov; 135(11):1263-1268.
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Adult nonketotic hyperglycinemia (NKH) crisis presenting as severe chorea and encephalopathy. Mov Disord. 2004 Apr; 19(4):485-6.
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Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH). Mol Genet Metab. 2003 Aug; 79(4):272-80.