{
    "disease_id": "DOID:0080633",
    "recommended_name": {
        "id": "DOID:0080633",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080633",
        "name": "developmental cardiac valvular defect",
        "description": "A physical disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PLD1 gene on chromosome 3q26."
    },
    "synonyms": [
        {
            "id": "MONDO:0008913",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008913",
            "name": "cardiac valvular defect, developmental",
            "description": ""
        },
        {
            "id": "MONDO:0008913",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008913",
            "name": "cardiac valvular defect, developmental",
            "description": ""
        },
        {
            "id": "MONDO:0008913",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008913",
            "name": "CVDD",
            "description": ""
        },
        {
            "id": "MIM:212093",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/212093",
            "name": "Cardiac valvular dysplasia 1",
            "description": "Cardiac valvular dysplasia 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080633"
    ],
    "unlinked_id_list": []
}