SLC35A1-CDG
id:
slc35a1-cdg-251-4785623
title:
SLC35A1-CDG
text:
SLC35A1-CDG is a rare inherited disorder that mainly affects the vascular systems of the body. It forms part of a large group of disorders called congenital disorders of glycosylation. It is caused by mutations in the SLC35A1 gene, located in the sixth chromosome.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/SLC35A1-CDG
date created:
date modified:
2023-10-27T15:08:40Z
main entity:
{"identifier":"Q60195113","url":"https://www.wikidata.org/entity/Q60195113"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/f/f1/Autosomal_recessive_-_en.svg","width":738,"height":1283}
fields total:
13
integrity:
15