{
    "disease_id": "DOID:0090029", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "infantile-onset multisystem inflammatory disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "IOMID syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "CINCA syndrome; CINCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "neonatal onset multisystem inflammatory disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "CINCA/NOMID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "Cryopyrin-associated periodic syndrome 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "NOMID syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "chronic infantile neurological cutaneous articular syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "CINCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "Prieur Griscelli syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "neonatal-onset multisystem inflammatory disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "multisystem inflammatory disease, neonatal-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "NOMID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "IOMID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "infantile onset multisystem inflammatory disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "chronic neurologic cutaneous and articular syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "chronic infantile neurological cutaneous and articular syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011776", 
            "name": "Prieur-Griscelli syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "IOMID syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "NOMID syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "Prieur-Griscelli syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "cryopyrin-associated periodic syndrome 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "infantile-onset multisystem inflammatory disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "neonatal-onset multisystem inflammatory disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "chronic infantile neurological cutaneous articular syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090029", 
            "name": "chronic neurologic cutaneous and articular syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090029", 
        "description": "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090029", 
        "name": "CINCA Syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090029#disease-associations", 
            "id": "0090029", 
            "database": "Alliance of Genome Resources"
        }
    ]
}