{
    "disease_id": "DOID:1657", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013749", 
            "name": "ventricular septal defect 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013749", 
            "name": "NKX2-5 ventricular septal defect (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013749", 
            "name": "ventricular septal defect (disease) caused by mutation in NKX2-5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013749", 
            "name": "ventricular septal defect type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013749", 
            "name": "VSD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013749", 
            "name": "ventricular septal defect 3; VSD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1657", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1657", 
            "name": "Interventricular septal defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1657", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1657", 
            "name": "Ventricular septal abnormality"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1657", 
        "description": "A heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1657", 
        "name": "ventricular septal defect"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/1657#disease-associations", 
            "id": "1657", 
            "database": "Alliance of Genome Resources"
        }
    ]
}