Term Name:	CINCA Syndrome
Synonyms:	chronic infantile neurological cutaneous articular syndrome, chronic neurologic cutaneous and articular syndrome, cryopyrin-associated periodic syndrome 3, infantile-onset multisystem inflammatory disease, IOMID syndrome, neonatal-onset multisystem inflammatory disease, NOMID syndrome, Prieur-Griscelli syndrome
Definition:	An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q.
Ontology:	Human Disease [DOID:0090029]   ( DOID:0090029 )