{
    "disease_id": "DOID:0051022",
    "recommended_name": {
        "id": "DOID:0051022",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051022",
        "name": "visceral heterotaxy 8",
        "description": "A visceral heterotaxy that is characterized by visceral situs inversus associated with complex congenital heart malformations caused by defects in the normal left-right asymmetric positioning of internal organs and that has_material_basis_in homozygous or compound heterozygous mutation in the PKD1L1 gene on chromosome 7p12."
    },
    "synonyms": [
        {
            "id": "MONDO:0014967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014967",
            "name": "heterotaxy, visceral, 8, autosomal",
            "description": "Any visceral heterotaxy in which the cause of the disease is a mutation in the PKD1L1 gene."
        },
        {
            "id": "MONDO:0014967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014967",
            "name": "HTX8",
            "description": ""
        },
        {
            "id": "MONDO:0014967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014967",
            "name": "PKD1L1 visceral heterotaxy",
            "description": ""
        },
        {
            "id": "MONDO:0014967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014967",
            "name": "heterotaxy, visceral, 8, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0014967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014967",
            "name": "heterotaxy, visceral, 8, autosomal; HTX8",
            "description": ""
        },
        {
            "id": "MONDO:0014967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014967",
            "name": "visceral heterotaxy caused by mutation in PKD1L1",
            "description": ""
        },
        {
            "id": "MIM:617205",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617205",
            "name": "Heterotaxy, visceral, 8, autosomal",
            "description": "Heterotaxy, visceral, 8, autosomal"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051022"
    ],
    "unlinked_id_list": []
}