{
    "disease_id": "DOID:0051024",
    "recommended_name": {
        "id": "DOID:0051024",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051024",
        "name": "visceral heterotaxy 10",
        "description": "A visceral heterotaxy that is characterized by a failure to generate normal left-right visceral asymmetry during embryogenesis, which can result in heterotaxy syndrome or situs inversus totalis and that has_material_basis_in homozygous mutation in the CFAP52 gene on chromosome 17p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0030474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030474",
            "name": "heterotaxy, visceral, 10, autosomal, with male infertility",
            "description": ""
        },
        {
            "id": "MONDO:0030474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030474",
            "name": "HTX10",
            "description": ""
        },
        {
            "id": "MIM:619607",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619607",
            "name": "Heterotaxy, visceral, 10, autosomal, with male infertility",
            "description": "Heterotaxy, visceral, 10, autosomal, with male infertility"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051024"
    ],
    "unlinked_id_list": []
}