Other Names for this Disease
- Alpha-aminoadipic semialdehyde synthase deficiency
- L-lysine NAD-oxido-reductase deficiency
- Lysine alpha-ketoglutarate reductase deficiency
- Lysine intolerance
- Lysine intolerance
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intellectual disability or behavioral problems. Hyperlysinemia is caused by mutations in the AASS gene. It has an autosomal recessive pattern of inheritance.Hyperlysinemia is an inherited condition characterized by elevated blood levels of the amino acid lysine. Hyperlysinemia typically causes no health problems, and most people with elevated lysine levels are unaware that they have this condition. Rarely, people with hyperlysinemia have
Last updated: 1/28/2013
- Hyperlysinemia. Genetics Home Reference (GHR). August 2009; http://ghr.nlm.nih.gov/condition=hyperlysinemia. Accessed 1/28/2013.
- Hyper LYS - Hyperlysinemia . Newborn Screening Coding and Terminology Guide. April 2011; http://newbornscreeningcodes.nlm.nih.gov/nb/sc/condition/Hyper-LYS. Accessed 1/28/2013.
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- Genetics Home Reference (GHR) contains information on Hyperlysinemia. This website is maintained by the National Library of Medicine.
- MeSH® (Medical Subject Headings) is a terminology tool used by the National Library of Medicine. Click on the link to view information on this topic.
- The Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
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