{
    "disease_id": "DOID:0050651", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013747", 
            "name": "atrioventricular septal defect 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013747", 
            "name": "AVSD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013747", 
            "name": "atrioventricular septal defect caused by mutation in GATA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013747", 
            "name": "GATA4 atrioventricular septal defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013747", 
            "name": "Atrioventricular septal defect type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013747", 
            "name": "ATRIOVENTRICULAR septal defect 4; AVSD4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050651", 
            "name": "AVCD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050651", 
            "name": "AVSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050651", 
            "name": "ECD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050651", 
            "name": "atrioventricular canal defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050651", 
            "name": "endocardial cushion defect"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050651", 
        "description": "A congenital heart septal defect characterized by an abnormal or inadequate fusion of the superior and inferior endocardial cushions with the mid portion of the atrial septum and the muscular portion of the ventricular septum, thus allowing extra blood to circulate the lungs.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050651", 
        "name": "atrioventricular septal defect"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050651#disease-associations", 
            "id": "0050651", 
            "database": "Alliance of Genome Resources"
        }
    ]
}