Hyperlysinemia

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Hyperlysinemia
L-lysine-skeletal.png
lysine
ICD-9 270.7
OMIM 238700
DiseasesDB 33215
MeSH D020167

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Hyperlysinemia is an autosomal recessive[1] metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It can be associated with saccharopine dehydrogenase.

Hyperlysinemia has an autosomal recessive pattern of inheritance.

See also

References

  1. Sacksteder KA, Bier BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT (2000). "Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia". American journal of human genetics. 66 (6): 1736–1743. doi:10.1086/302919. PMC 1378037. PMID 10775527. Unknown parameter |month= ignored (help)

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