Hyperlysinemia

Hyperlysinemia

Infobox_Disease
Name = PAGENAME



Caption = lysine
DiseasesDB = 33215
ICD10 =
ICD9 = ICD9|270.7
ICDO =
OMIM = 238700
MedlinePlus =
eMedicineSubj =
eMedicineTopic =
MeshID = D020167

Hyperlysinemia is an autosomal recessive [cite journal |pmid=10775527 |year=2000 |month=Jun |author=Sacksteder KA, Bier BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT |title=Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia |volume=66 |issue=6 |pages=1736-1743 |pmc=1378037 |doi=10.1086/302919 |journal=American journal of human genetics] metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It can be associated with saccharopine dehydrogenase.

See also

* Lysinuria
* Saccharopinuria

References


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