{
    "disease_id": "DOID:0050854",
    "recommended_name": {
        "id": "DOID:0050854",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050854",
        "name": "Muckle-Wells syndrome",
        "description": "A syndrome characterized by episodic skin rash, arthralgias, and fever associated with late-onset sensorineural deafness and renal amyloidosis that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q44."
    },
    "synonyms": [
        {
            "id": "DOID:0050854",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050854",
            "name": "MWS",
            "description": ""
        },
        {
            "id": "DOID:0050854",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050854",
            "name": "neutrophilic urticaria",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "Muckle-Wells syndrome",
            "description": "An intermediate form of cryopyrin-associated periodic syndrome (CAPS) and is characterized by recurrent fever (with malaise and chills), recurrent urticaria-like skin rash, sensorineural deafness, general signs of inflammation (eye redness, headaches, arthralgia/myalgia) and potentially life-threatening secondary amyloidosis (AA type)."
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "Muckle-Wells syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "neutrophilic urticaria",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "Cryopyrin-associated periodic syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "MUCKLE-Wells syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "MWS",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "Muckle Wells syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "Uda syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "urticaria, deafness and amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0008633",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008633",
            "name": "urticaria-deafness-amyloidosis syndrome",
            "description": ""
        },
        {
            "id": "MIM:191900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/191900",
            "name": "Muckle-Wells syndrome",
            "description": "Muckle-Wells syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050854"
    ],
    "unlinked_id_list": []
}