 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.
| Descriptor ID |
D020158
|
| 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 UAMS Profiles by year, and whether "Hyperglycinemia, Nonketotic" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2019 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2000 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Hyperglycinemia, Nonketotic" by people in Profiles over the past ten years.
-
Shbarou RM, Boustany RM, Daher RT, Pakdel P, Noureddine A, Karam PE. Outcome of Nonketotic Hyperglycinemia in Lebanon: 14-Year Retrospective Review. Neuropediatrics. 2019 08; 50(4):235-243.
-
Silverstein S, Veerapandiyan A, Hayes-Rosen C, Ming X, Kornitzer J. A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia. Metab Brain Dis. 2019 02; 34(1):373-376.
-
Alfadhel M, Nashabat M, Qahtani HA, Alfares A, Mutairi FA, Shaalan HA, Douglas GV, Wierenga K, Juusola J, Alrifai MT, Arold ST, Alkuraya F, Ali QA. 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.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|