{
    "disease_id": "DOID:0051020",
    "recommended_name": {
        "id": "DOID:0051020",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051020",
        "name": "visceral heterotaxy 6",
        "description": "A visceral heterotaxy that is has_material_basis_in homozygous mutation in the CCDC11 gene (CFAP53) on chromosome 18q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "heterotaxy, visceral, 6, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "heterotaxy, visceral, 6, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "heterotaxy, visceral, 6, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "HTX6",
            "description": ""
        },
        {
            "id": "MIM:614779",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614779",
            "name": "Heterotaxy, visceral, 6, autosomal",
            "description": "Heterotaxy, visceral, 6, autosomal"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051020"
    ],
    "unlinked_id_list": []
}