2,4 Dienoyl-CoA reductase deficiency
id:
2-4-dienoyl-coa-reductase-deficiency-192-8065806
title:
2,4 Dienoyl-CoA reductase deficiency
text:
2,4 Dienoyl-CoA reductase deficiency is an inborn error of metabolism resulting in defective fatty acid oxidation caused by a deficiency of the enzyme 2,4 Dienoyl-CoA reductase. Lysine degradation is also affected in this disorder leading to hyperlysinemia. The disorder is inherited in an autosomal recessive manner, meaning an individual must inherit mutations in NADK2, located at 5p13.2 from both of their parents. NADK2 encodes the mitochondrial NAD kinase. A defect in this enzyme leads to defi
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/2,4_Dienoyl-CoA_reductase_deficiency
date created:
date modified:
2024-01-28T22:57:43Z
main entity:
{"identifier":"Q4596783","url":"https://www.wikidata.org/entity/Q4596783"}
image:
fields total:
13
integrity:
14