{
    "disease_id": "DOID:0060297", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013721", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013721", 
            "name": "C4AD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013721", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013721", 
            "name": "C4A classic complement early component deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013721", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013721", 
            "name": "classic complement early component deficiency caused by mutation in C4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013721", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013721", 
            "name": "C4A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013721", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013721", 
            "name": "complement component 4A deficiency; C4AD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060297", 
        "description": "A complement deficiency that is characterized by recurrnet bascterial infections, caused by C4A deficiency.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060297", 
        "name": "complement component 4a deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614380", 
            "id": "614380", 
            "database": "MIM"
        }
    ]
}