{
    "disease_id": "DOID:0080633", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008913", 
            "name": "cardiac valvular defect, developmental"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008913", 
            "name": "CVDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008913", 
            "name": "CARDIAC valvular defect, developmental; CVDD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080633", 
        "description": "A physical disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PLD1 gene on chromosome 3q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080633", 
        "name": "developmental cardiac valvular defect"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080633#disease-associations", 
            "id": "0080633", 
            "database": "Alliance of Genome Resources"
        }
    ]
}