{
    "disease_id": "DOID:0110108", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013567", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013567", 
            "name": "atrial heart septal defect type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013567", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013567", 
            "name": "atrial heart septal defect caused by mutation in MYH6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013567", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013567", 
            "name": "ASD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013567", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013567", 
            "name": "MYH6 atrial heart septal defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013567", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013567", 
            "name": "atrial septal defect type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013567", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013567", 
            "name": "atrial septal defect 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013567", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013567", 
            "name": "atrial septal defect 3; ASD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110108", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110108", 
            "name": "ASD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110108", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110108", 
            "name": "atrial septal defect 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110108", 
        "description": "An atrial heart septal defect type 3 that has_material_basis_in heterozygous mutation in the myosin heavy chain-6 gene (MYH6) on chromosome 14q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110108", 
        "name": "atrial heart septal defect 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110108#disease-associations", 
            "id": "0110108", 
            "database": "Alliance of Genome Resources"
        }
    ]
}