Hyperlysinemia
id:
hyperlysinemia-271-12235660
title:
Hyperlysinemia
text:
Hyperlysinemia is an autosomal recessive metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It is caused by mutations in AASS, which encodes α-aminoadipic semialdehyde synthase. Hyperlysinemia is associated with ectopia lentis in humans.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Hyperlysinemia
date created:
date modified:
2023-12-03T16:04:09Z
main entity:
{"identifier":"Q10295763","url":"https://www.wikidata.org/entity/Q10295763"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/0/04/L-lysine-skeletal.png","width":1977,"height":1462}
fields total:
13
integrity:
15