{
    "disease_id": "DOID:0060002",
    "recommended_name": {
        "id": "DOID:0060002",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060002",
        "name": "C1 inhibitor deficiency",
        "description": "A complement deficiency that is a functional deficiency in the complement component C1 inhibitor leading to hereditary angioedema (HAE) involving swelling due to leakage of fluid from blood vessels into connective tissue."
    },
    "synonyms": [
        {
            "id": "DOID:0060002",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060002",
            "name": "Quincke edema",
            "description": ""
        },
        {
            "id": "MONDO:0007361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007361",
            "name": "C1 inhibitor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007361",
            "name": "Quincke edema",
            "description": ""
        },
        {
            "id": "MONDO:0007361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007361",
            "name": "complement component 4, partial deficiency OF",
            "description": ""
        }
    ]
}
