{
    "disease_id": "DOID:0051023",
    "recommended_name": {
        "id": "DOID:0051023",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051023",
        "name": "visceral heterotaxy 9",
        "description": "A visceral heterotaxy that is characterized by randomization of organ laterality, resulting in defects such as situs inversus and dextrocardia and that has_material_basis_in homozygous mutation in the MNS1 gene on chromosome 15q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0030070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030070",
            "name": "heterotaxy, visceral, 9, autosomal, with male infertility",
            "description": ""
        },
        {
            "id": "MONDO:0030070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030070",
            "name": "HETEROTAXY, VISCERAL, 9, AUTOSOMAL, WITH MALE INFERTILITY",
            "description": ""
        },
        {
            "id": "MONDO:0030070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030070",
            "name": "HTX9",
            "description": ""
        },
        {
            "id": "MONDO:0030070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030070",
            "name": "heterotaxy, visceral, 9, autosomal, with male infertility",
            "description": ""
        },
        {
            "id": "MIM:618948",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618948",
            "name": "Heterotaxy, visceral, 9, autosomal, with male infertility",
            "description": "Heterotaxy, visceral, 9, autosomal, with male infertility"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051023"
    ],
    "unlinked_id_list": []
}