Contiguous gene syndrome
id:
contiguous-gene-syndrome-285-7300143
title:
Contiguous gene syndrome
text:
A contiguous gene syndrome (CGS), also known as a contiguous gene deletion syndrome, is a clinical phenotype caused by a chromosomal abnormality, such as a deletion or duplication that removes several genes lying in close proximity to one another on the chromosome. The combined phenotype of the patient is a combination of what is seen when any individual has disease-causing mutations in any of the individual genes involved in the deletion. While it can be caused by deleted material on a chromoso
brand slug:
wiki
category slug:
encyclopedia
description:
Combined clinical phenotype caused by each gene involved in a chromosomal abnormality
original url:
https://en.wikipedia.org/wiki/Contiguous_gene_syndrome
date created:
date modified:
2022-10-01T21:18:10Z
main entity:
{"identifier":"Q1128743","url":"https://www.wikidata.org/entity/Q1128743"}
image:
fields total:
13
integrity:
14