MPI-CDG
id:
mpi-cdg-195-3527272
title:
MPI-CDG
text:
MPI-CDG is an autosomal recessive congenital disorder of glycosylation caused by biallelic pathogenic variants in MPI. The clinical symptoms in MPI-CDG are caused by deficient activity of the enzyme mannose phosphate isomerase. Clinically, the most common symptoms of MPI-CDG are chronic diarrhea, failure to thrive, protein-losing enteropathy, and coagulopathy. MPI-CDG differs from most other described glycosylation disorders due to its lack of central nervous system involvement, and because it h
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/MPI-CDG
date created:
date modified:
2023-08-13T01:53:52Z
main entity:
{"identifier":"Q65066312","url":"https://www.wikidata.org/entity/Q65066312"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/1/11/Mannose_structure.svg","width":512,"height":314}
fields total:
13
integrity:
15