Blau syndrome
id:
blau-syndrome-180-17720424
title:
Blau syndrome
text:
Blau syndrome is an autosomal dominant genetic inflammatory disorder which affects the skin, eyes, and joints. It is caused by a mutation in the NOD2 (CARD15) gene. and is classified as an inborn errors of immunity. Symptoms usually begin before the age of four, and the disease manifests as early onset cutaneous sarcoidosis, granulomatous arthritis, and uveitis.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Blau_syndrome
date created:
2008-12-19T21:38:37Z
date modified:
2024-09-05T15:07:43Z
main entity:
{"identifier":"Q441077","url":"https://www.wikidata.org/entity/Q441077"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/e/e3/Blau_syndrome2.jpg","width":640,"height":853}
fields total:
13
integrity:
16