DO_rare_slim has material basis in autosomal dominant disease CINCA Syndrome 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. DOID:0090029 ICD10CM:E85.0 IOMID syndrome ORDO:1451 MIM:607115 NOMID syndrome chronic infantile neurological cutaneous articular syndrome chronic neurologic cutaneous and articular syndrome cryopyrin-associated periodic syndrome 3 disease_ontology Prieur-Griscelli syndrome infantile-onset multisystem inflammatory disease neonatal-onset multisystem inflammatory disease autoimmune disease autosomal dominant inheritance