{
    "disease_id": "DOID:0051027",
    "recommended_name": {
        "id": "DOID:0051027",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051027",
        "name": "visceral heterotaxy 13",
        "description": "A visceral heterotaxy that is characterized by heterotaxy and congenital heart disease and that has_material_basis_in homozygous mutation in the DAND5 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0051027",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0051027",
            "name": "HTX13",
            "description": ""
        },
        {
            "id": "MONDO:0976134",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0976134",
            "name": "heterotaxy, visceral, 13, autosomal",
            "description": ""
        },
        {
            "id": "MIM:621079",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/621079",
            "name": "Heterotaxy, visceral, 13, autosomal",
            "description": "Heterotaxy, visceral, 13, autosomal"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051027"
    ],
    "unlinked_id_list": []
}