 Brain Diseases, Metabolic, Inborn
"Brain Diseases, Metabolic, Inborn" 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.
Brain disorders resulting from inborn metabolic errors, primarily from enzymatic defects which lead to substrate accumulation, product reduction, or increase in toxic metabolites through alternate pathways. The majority of these conditions are familial, however spontaneous mutation may also occur in utero.
| Descriptor ID |
D020739
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| MeSH Number(s) |
C10.228.140.163.100 C16.320.565.189 C18.452.132.100 C18.452.648.189
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| Concept/Terms |
Brain Diseases, Metabolic, Inborn- Brain Diseases, Metabolic, Inborn
- Encephalopathies, Metabolic, Inborn
- Inborn Errors of Metabolism, Brain
- Metabolic Diseases, Inborn, Brain
- Inborn Metabolic Brain Disorders
- Inborn Metabolic Disorders, Brain
- Metabolic Brain Diseases, Inborn
- Metabolic Brain Syndrome, Inborn
- Brain Syndrome, Metabolic, Inborn
- Inborn Metabolic Brain Diseases
Central Nervous System Inborn Metabolic Diseases- Central Nervous System Inborn Metabolic Diseases
- Metabolic Disorders, CNS, Inborn
- Metabolic Diseases, Inborn, Central Nervous System
- Central Nervous System Inborn Metabolic Disorders
- CNS Metabolic Disorders, Inborn
Brain Diseases, Metabolic, Inherited- Brain Diseases, Metabolic, Inherited
- Familial Metabolic Brain Diseases
- Familial Metabolic Disorders, Brain
- Metabolic Disorders, Familial, Brain
- Inherited Metabolic Disorders, Brain
- Metabolic Brain Diseases, Familial
- Metabolic Brain Diseases, Inherited
- Metabolic Disorders, Brain, Inherited
- Brain Diseases, Metabolic, Familial
- Inherited Metabolic Brain Diseases
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Below are MeSH descriptors whose meaning is more general than "Brain Diseases, Metabolic, Inborn".
- 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]
- 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]
- Metabolism, Inborn Errors [C18.452.648]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
Below are MeSH descriptors whose meaning is more specific than "Brain Diseases, Metabolic, Inborn".
This graph shows the total number of publications written about "Brain Diseases, Metabolic, Inborn" by people in UAMS Profiles by year, and whether "Brain Diseases, Metabolic, Inborn" 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 |
|---|
| 2020 | 1 | 0 | 1 | | 2005 | 1 | 0 | 1 |
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Below are the most recent publications written about "Brain Diseases, Metabolic, Inborn" by people in Profiles over the past ten years.
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Srinivasan A, Zhou Y, Scordino T, Prabhu S, Wierenga A, Simon G, Wierenga KJ, Thompson J, Shah R, Sinha AA. IDH1 mutated acute myeloid leukemia in a child with metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria. Pediatr Hematol Oncol. 2020 Aug; 37(5):431-437.
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