Mahvash disease
id:
mahvash-disease-232-11713323
title:
Mahvash disease
text:
Mahvash disease is an autosomal recessive, hereditary pancreatic neuroendocrine tumor syndrome. The genetic defect that causes Mahvash disease is biallelic inactivating mutations of the glucagon receptor gene (GCGR). Mahvash disease was discovered by American physician Run Yu and his colleagues in 2008. Mahvash disease is very rare. There have been approximately 15 cases of Mahvash disease described in detail by the end of 2023. Mahvash disease occurs in both females and males. Mahvash disease i
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Mahvash_disease
date created:
date modified:
2024-01-04T14:58:36Z
main entity:
{"identifier":"Q55788193","url":"https://www.wikidata.org/entity/Q55788193"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/en/e/e0/Mahvash_disease.tif","width":1280,"height":1024}
fields total:
13
integrity:
15