Cryopyrin is a recently discovered
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cryopyrin — cryo·py·rin (kri″o piґrin) a complex protein containing a pyrin domain, a nucleotide binding site, and a leucine rich repeat domain, found in inflammasomes. See also cryopyrin associated periodic syndrome … Medical dictionary
Cryopyrin-associated periodic syndrome — Classification and external resources MeSH D056587 Cryopyrin associated periodic syndrome (CAPS) is a spectrum of autoinflammatory syndromes including familial cold autoinflammatory syndrome (FCAS, formerly termed familial cold induced urticaria) … Wikipedia
cryopyrin-associated periodic syndrome — any in a group of autoinflammatory diseases caused by mutations in the gene that codes for cryopyrin, resulting in fever, arthralgia, urticaria, and inflammation. Called also cryopyrinopathy … Medical dictionary
cryopyrin — noun A nucleotide binding and leucin rich protein which activates the inflammasome in response to toxins … Wiktionary
Muckle-Wells syndrome — Infobox Disease Name = Muckle Wells syndrome Caption = DiseasesDB = 30159 ICD10 = ICD10|E|85|0|e|75, ICD10|L|50|8|l|50 ICD9 = ICD9|xxx ICDO = OMIM = 191900 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Muckle Wells syndrome (MWS), also… … Wikipedia
NALP3 — NLR family, pyrin domain containing 3 Identifiers Symbols NLRP3; AGTAVPRL; AII; AII/AVP; AVP; C1orf7; CIAS1; CLR1.1; FCAS; FCU; FLJ95925; MWS; NALP3; PYPAF1 External IDs … Wikipedia
Muckle–Wells syndrome — Classification and external resources ICD 10 Template:ICD10E, L50.8 OMIM 191900 … Wikipedia
CIAS1 — NLR family, pyrin domain containing 3, also known as NLRP3, is a human gene.cite web | title = Entrez Gene: NLRP3 NLR family, pyrin domain containing 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
Rilonacept — drugbox IUPAC name = n/a CAS number = ATC prefix = L04 ATC suffix = AC04 PubChem = DrugBank = molecular weight = bioavailability = metabolism = elimination half life = excretion = pregnancy US = C legal UK = legal US = Rx only legal status =… … Wikipedia
Muckle-Wells-Syndrom — Das Muckle Wells Syndrom ist eine seltene, autosomal dominant vererbte Autoimmunerkrankung. Sie ist nach Thomas James Muckle und Michael Vernon Wells benannt, die sie im Jahr 1962 erstbeschrieben. Inhaltsverzeichnis 1 Symptome 2 Pathogenese 3… … Deutsch Wikipedia
