Hyperlysinemias
"Hyperlysinemias" 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.
A group of inherited metabolic disorders which have in common elevations of serum LYSINE levels. Enzyme deficiencies of alpha-aminoadipic semialdehyde dehydrogenase and the SACCHAROPINE DEHYDROGENASES have been associated with hyperlysinemia. Clinical manifestations include mental retardation, recurrent emesis, hypotonia, lethargy, diarrhea, and developmental delay. (From Menkes, Textbook of Child Neurology, 5th ed, p56)
Descriptor ID |
D020167
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MeSH Number(s) |
C10.228.140.163.100.380 C16.320.565.100.544 C16.320.565.189.380 C18.452.132.100.380 C18.452.648.100.544 C18.452.648.189.380
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Concept/Terms |
Hyperlysinemias- Hyperlysinemias
- Hyperlysinemia
- L-Lysine:NAD-Oxido-Reductase Deficiency
- Deficiencies, L-Lysine:NAD-Oxido-Reductase
- Deficiency, L-Lysine:NAD-Oxido-Reductase
- L Lysine:NAD Oxido Reductase Deficiency
- L-Lysine:NAD-Oxido-Reductase Deficiencies
- Lysine:Alpha-Ketoglutarate Reductase Deficiency
- Deficiencies, Lysine:Alpha-Ketoglutarate Reductase
- Deficiency, Lysine:Alpha-Ketoglutarate Reductase
- Lysine:Alpha Ketoglutarate Reductase Deficiency
- Lysine:Alpha-Ketoglutarate Reductase Deficiencies
- Reductase Deficiencies, Lysine:Alpha-Ketoglutarate
- Reductase Deficiency, Lysine:Alpha-Ketoglutarate
- Familial Hyperlysinemia
- Hyperlysinemia, Familial
- Familial Hyperlysinemias
- Hyperlysinemias, Familial
Hyperlysinemia, Periodic- Hyperlysinemia, Periodic
- Hyperlysinemias, Periodic
- Periodic Hyperlysinemia
- Periodic Hyperlysinemias
- Hyperlysinuria With Hyperammonemia
- Hyperammonemia, Hyperlysinuria With
- Hyperammonemias, Hyperlysinuria With
- Hyperlysinuria With Hyperammonemias
- With Hyperammonemia, Hyperlysinuria
- With Hyperammonemias, Hyperlysinuria
Alpha-Aminoadipic Semialdehyde Deficiency Disease- Alpha-Aminoadipic Semialdehyde Deficiency Disease
- Alpha Aminoadipic Semialdehyde Deficiency Disease
- Deficiency Disease, Alpha-Aminoadipic Semialdehyde
- Deficiency Disease, Alpha Aminoadipic Semialdehyde
Lysine Alpha-Ketoglutarate Reductase Deficiency Disease- Lysine Alpha-Ketoglutarate Reductase Deficiency Disease
- Lysine Alpha Ketoglutarate Reductase Deficiency Disease
- Deficiency Disease, Lysine Alpha-Ketoglutarate Reductase
- Deficiency Disease, Lysine Alpha Ketoglutarate Reductase
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Below are MeSH descriptors whose meaning is more general than "Hyperlysinemias".
- 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]
- Hyperlysinemias [C10.228.140.163.100.380]
- 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]
- Hyperlysinemias [C16.320.565.100.544]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Hyperlysinemias [C16.320.565.189.380]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Hyperlysinemias [C18.452.132.100.380]
- Metabolism, Inborn Errors [C18.452.648]
- Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
- Hyperlysinemias [C18.452.648.100.544]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Hyperlysinemias [C18.452.648.189.380]
Below are MeSH descriptors whose meaning is more specific than "Hyperlysinemias".
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