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- Q1538218 subject Q6853484.
- Q1538218 subject Q7064928.
- Q1538218 subject Q8279947.
- Q1538218 abstract "Muckle–Wells syndrome (MWS), also known as (UDA), is a rare autosomal dominant disease which causes sensorineural deafness, recurrent hives, and can lead to amyloidosis. Individuals with MWS often have episodic fever, chills, and joint pain. As a result, MWS is considered a type of periodic fever syndrome. MWS is caused by a defect in the CIAS1 gene which creates the protein cryopyrin. MWS is closely related to two other syndromes, familial cold urticaria and neonatal onset multisystem inflammatory disease—in fact, all three are related to mutations in the same gene and subsumed under the term cryopyrin-associated periodic syndromes (CAPS).".
- Q1538218 icd10 "E85.0,L50.8".
- Q1538218 meshId "D056587".
- Q1538218 omim "191900".
- Q1538218 wikiPageExternalLink www.NOMIDAlliance.net.
- Q1538218 wikiPageExternalLink muckle-wells-syndrome.
- Q1538218 wikiPageWikiLink Q101991.
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- Q1538218 wikiPageWikiLink Q422248.
- Q1538218 wikiPageWikiLink Q6531938.
- Q1538218 wikiPageWikiLink Q683498.
- Q1538218 wikiPageWikiLink Q6853484.
- Q1538218 wikiPageWikiLink Q7064928.
- Q1538218 wikiPageWikiLink Q7302381.
- Q1538218 wikiPageWikiLink Q7334300.
- Q1538218 wikiPageWikiLink Q779203.
- Q1538218 wikiPageWikiLink Q7901363.
- Q1538218 wikiPageWikiLink Q8054.
- Q1538218 wikiPageWikiLink Q816798.
- Q1538218 wikiPageWikiLink Q8279947.
- Q1538218 wikiPageWikiLink Q928697.
- Q1538218 wikiPageWikiLink Q929833.
- Q1538218 icd "E85.0, L50.8".
- Q1538218 meshid "D056587".
- Q1538218 name "Muckle–Wells syndrome".
- Q1538218 omim "191900".
- Q1538218 type Disease.
- Q1538218 type Thing.
- Q1538218 type Q12136.
- Q1538218 comment "Muckle–Wells syndrome (MWS), also known as (UDA), is a rare autosomal dominant disease which causes sensorineural deafness, recurrent hives, and can lead to amyloidosis. Individuals with MWS often have episodic fever, chills, and joint pain. As a result, MWS is considered a type of periodic fever syndrome. MWS is caused by a defect in the CIAS1 gene which creates the protein cryopyrin.".
- Q1538218 label "Muckle–Wells syndrome".
- Q1538218 name "Muckle–Wells syndrome".