CINCA syndrome
Sign in to saveAlso known as NOMID syndrome, chronic infantile neurological cutaneous articular syndrome, Prieur-Griscelli syndrome, infantile-onset multisystem inflammatory disease, cryopyrin-associated periodic syndrome 3, IOMID syndrome, chronic neurologic cutaneous and articular syndrome, neonatal-onset multisystem inflammatory disease
Chronic Infantile Neurological, Cutaneous, and Articular (CINCA) syndrome is characterised by skin rash, joint involvement, chronic meningitis with granulocytes and, in some cases, sensorineural hearing loss and ocular signs
In the Vinony graph
Vinony's link graph records 19 inbound references to CINCA syndrome, and connects out to anemia, meninges and granulocyte.
It is catalogued under topics including Neonatology, Rare diseases and Rheumatology.
Vinony links it to 6 Wikipedia language editions.
Wikidata facts
Show 6 more facts
- health specialty
- rheumatology
- exact match
- www.orpha.net/ORDO/Orphanet_1451
- NCI Thesaurus ID
- C116380
- ICD-9-CM
- 759.89
- genetic association
- NLRP3
- on focus list of Wikimedia project
- WikiProject Medicine
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