{
    "disease_id": "DOID:0070719",
    "recommended_name": {
        "id": "DOID:0070719",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070719",
        "name": "neurocardiorenal malformation syndrome",
        "description": "A physical disorder characterized by severe developmental delay associated with microcephaly, distinctive facial features, and multiorgan involvement including cardiac and renal malformations that has_material_basis_in homozygous or compound heterozygous mutation in the TM2D3 gene on chromosome 15q26."
    },
    "synonyms": [
        {
            "id": "MONDO:0980704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980704",
            "name": "neurocardiorenal malformation syndrome",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070719"
    ],
    "unlinked_id_list": []
}