{
    "disease_id": "DOID:8354", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013417", 
            "name": "complement component 3 deficiency, autosomal recessive; C3d"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013417", 
            "name": "C3 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013417", 
            "name": "complement component 3 deficiency, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013417", 
            "name": "C3 deficiency, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013417", 
            "name": "classic complement early component deficiency caused by mutation in C3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013417", 
            "name": "C3d"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013417", 
            "name": "C3 classic complement early component deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:8354", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:8354", 
            "name": "C3 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:8354", 
        "description": "A complement deficiency that is characterized by deficiency of complement component 3 that increases susceptibility to infection and autoimmune diseases and has_material_basis_in autosomal recessive inheritance of mutation in the C3 gene on chromosome 19p13.3, has_symptom recurrent bacterial infections.", 
        "resource": "Disease Ontology", 
        "id": "DOID:8354", 
        "name": "complement component 3 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613779", 
            "id": "613779", 
            "database": "MIM"
        }
    ]
}