GFER syndrome
id:
gfer-syndrome-257-10506050
title:
GFER syndrome
text:
GFER syndrome is a rare mitochondrial disease. GFER was first reported in 2009 and since exome sequencing became more available, more cases were discovered. In all known cases, the disease progresses with conditions that include: congenital cataracts, loss of motor abilities, development delay, degeneration of organs, sometimes hearing loss, etc.
brand slug:
wiki
category slug:
encyclopedia
description:
Rare disease
original url:
https://en.wikipedia.org/wiki/GFER_syndrome
date created:
date modified:
2024-02-24T05:14:27Z
main entity:
{"identifier":"Q55612180","url":"https://www.wikidata.org/entity/Q55612180"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/f/f1/Autosomal_recessive_-_en.svg","width":738,"height":1283}
fields total:
13
integrity:
15