Structured Summary
Abstract
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)
MeSH Record
Classification
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
See Also
MeSH Record
Synonyms
37 entry terms
- Familial Hyperlysinemia
- Hyperlysinemia
- Hyperlysinemia, Familial
- L-Lysine:NAD-Oxido-Reductase Deficiency
- Lysine:Alpha-Ketoglutarate Reductase Deficiency
- Deficiencies, L-Lysine:NAD-Oxido-Reductase
- Deficiencies, Lysine:Alpha-Ketoglutarate Reductase
- Deficiency, L-Lysine:NAD-Oxido-Reductase
- Deficiency, Lysine:Alpha-Ketoglutarate Reductase
- Familial Hyperlysinemias
- Hyperlysinemias, Familial
- L Lysine:NAD Oxido Reductase Deficiency
- L-Lysine:NAD-Oxido-Reductase Deficiencies
- Lysine:Alpha Ketoglutarate Reductase Deficiency
- Lysine:Alpha-Ketoglutarate Reductase Deficiencies
- Reductase Deficiencies, Lysine:Alpha-Ketoglutarate
- Reductase Deficiency, Lysine:Alpha-Ketoglutarate
- Alpha-Aminoadipic Semialdehyde Deficiency Disease
- Deficiency Disease, Alpha-Aminoadipic Semialdehyde
- Deficiency Disease, Lysine Alpha-Ketoglutarate Reductase
- Deficiency Disease, Saccharopine Dehydrogenase
- Hyperlysinemia, Periodic
- Hyperlysinuria With Hyperammonemia
- Lysine Alpha-Ketoglutarate Reductase Deficiency Disease
- Saccharopine Dehydrogenase Deficiency Disease
- Alpha Aminoadipic Semialdehyde Deficiency Disease
- Deficiency Disease, Alpha Aminoadipic Semialdehyde
- Deficiency Disease, Lysine Alpha Ketoglutarate Reductase
- Hyperammonemia, Hyperlysinuria With
- Hyperammonemias, Hyperlysinuria With
- Hyperlysinemias, Periodic
- Hyperlysinuria With Hyperammonemias
- Lysine Alpha Ketoglutarate Reductase Deficiency Disease
- Periodic Hyperlysinemia
- Periodic Hyperlysinemias
- With Hyperammonemia, Hyperlysinuria
- With Hyperammonemias, Hyperlysinuria
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2000
MeSH Record
Previous Indexing
- Amino Acid Metabolism, Inborn Errors (1965-1999)
- Lysine/metabolism (1966-1999)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Hyperlysinemias. Medical Subject Headings (MeSH). 2026. Unique ID D020167. http://id.nlm.nih.gov/mesh/2026/D020167
- Hyperlysinemias. In: Wikipedia. https://en.wikipedia.org/wiki/Hyperlysinemia
- Hyperlysinemias. In: Wikidata. https://www.wikidata.org/wiki/Q10295763