Hyperlysinemia

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Hyperlysinemia
Classification and external resources
lysine
ICD-9 270.7
OMIM 238700
DiseasesDB 33215
MeSH D020167

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.
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 (Jun 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. PMID 10775527. 
v • d • e
Inborn errors of amino acid metabolism (E70-72, 270)
K
Lysine/straight chain
G→pyruvate
G→alpha-ketoglutarate
G→succinyl-CoA
General BC/OA
G→fumarate
G→oxaloacetate
Transport
Tyrosine→Melanin
Glycine→Creatine
Other
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  • This page was last modified on 27 July 2008, at 01:25.

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