CINCA syndrome
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
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CINCA syndrome
Summary
CINCA syndrome is a rare disease[1]. It draws 10 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2]
Key Facts
- CINCA syndrome's instance of is recorded as rare disease[3].
- CINCA syndrome's instance of is recorded as class of disease[4].
- CINCA syndrome is a type of cryopyrin-associated periodic syndrome[5].
- CINCA syndrome is a type of autoimmune disease[6].
- CINCA syndrome is a type of rare genetic eye disease[7].
- CINCA syndrome is a type of systemic diseases with anterior uveitis[8].
- CINCA syndrome is a type of genetic disease[9].
- CINCA syndrome is a type of autosomal dominant disease[10].
- CINCA syndrome's ICD-9-CM is recorded as 759.89[11].
- CINCA syndrome's NCI Thesaurus ID is recorded as C116380[12].
- CINCA syndrome's health specialty is recorded as neurology[13].
- CINCA syndrome's health specialty is recorded as dermatology[14].
- CINCA syndrome's health specialty is recorded as rheumatology[15].
- CINCA syndrome's genetic association is recorded as NLRP3[16].
- CINCA syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090029[17].
- CINCA syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090029[18].
- CINCA syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1451[19].
- CINCA syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
CINCA syndrome draws 10 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[21] It is known by 20 alternative names across languages and contexts.[22]