{
    "disease_id": "DOID:0061180",
    "recommended_name": {
        "id": "DOID:0061180",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061180",
        "name": "familial hypercholanemia 3",
        "description": "A steroid inherited metabolic disorder characterized by onset of symptoms, including jaundice and failure to thrive, in early infancy that has_material_basis_in homozygous or compound heterozygous mutation in the BAAT gene on chromosome 9q31."
    },
    "synonyms": [
        {
            "id": "MONDO:0030991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030991",
            "name": "bile acid conjugation defect 1",
            "description": ""
        },
        {
            "id": "MONDO:0030991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030991",
            "name": "BACD1",
            "description": ""
        },
        {
            "id": "MIM:619232",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619232",
            "name": "Hypercholanemia, familial 3",
            "description": "Hypercholanemia, familial 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061180"
    ],
    "unlinked_id_list": []
}