{
    "disease_id": "DOID:0090029",
    "recommended_name": {
        "id": "DOID:0090029",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0090029",
        "name": "CINCA Syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "IOMID syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "NOMID syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "Prieur-Griscelli syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "cryopyrin-associated periodic syndrome 3",
            "description": ""
        },
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "infantile-onset multisystem inflammatory disease",
            "description": ""
        },
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "neonatal-onset multisystem inflammatory disease",
            "description": ""
        },
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "chronic infantile neurological cutaneous articular syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090029",
            "name": "chronic neurologic cutaneous and articular syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "CINCA syndrome",
            "description": "Chronic Infantile Neurological, Cutaneous, and Articular (CINCA) syndrome is characterized by skin rash, joint involvement, chronic meningitis with granulocytes and, in some cases, sensorineural hearing loss and ocular signs."
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "CINCA syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "CINCA/NOMID",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "IOMID syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "NOMID",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "NOMID syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "Neonatal-Onset Multisystem Inflammatory Disease",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "Prieur-Griscelli syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "chronic infantile neurological cutaneous and articular syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "chronic infantile neurological cutaneous articular syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "chronic neurologic cutaneous and articular syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "cryopyrin-associated periodic syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "infantile-onset multisystem inflammatory disease",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "neonatal-onset multisystem inflammatory disease",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "CINCA",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "Cryopyrin-associated periodic syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "IOMID",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "Prieur Griscelli syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "infantile onset multisystem inflammatory disease",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "multisystem inflammatory disease, neonatal-onset",
            "description": ""
        },
        {
            "id": "MONDO:0011776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011776",
            "name": "neonatal onset multisystem inflammatory disease",
            "description": ""
        },
        {
            "id": "MIM:607115",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607115",
            "name": "Chronic infantile neurologic cutaneous and articular syndrome",
            "description": "Chronic infantile neurologic cutaneous and articular syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0090029"
    ],
    "unlinked_id_list": []
}