{
    "disease_id": "DOID:0061182",
    "recommended_name": {
        "id": "DOID:0061182",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061182",
        "name": "familial hypercholanemia 2",
        "description": "A steroid inherited metabolic disorder characterized by persistently increased plasma levels of conjugated bile salts apparent from infancy that has_material_basis_in homozygous or compound heterozygous mutation in the SLC10A1 gene on chromosome 14q24."
    },
    "synonyms": [
        {
            "id": "MONDO:0031003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031003",
            "name": "hypercholanemia, familial, 2",
            "description": ""
        },
        {
            "id": "MONDO:0031003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031003",
            "name": "FHCA2",
            "description": ""
        },
        {
            "id": "MONDO:0031003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031003",
            "name": "NTCP Deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0031003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031003",
            "name": "hypercholanemia, familial 2",
            "description": ""
        },
        {
            "id": "MIM:619256",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619256",
            "name": "Hypercholanemia, familial, 2",
            "description": "Hypercholanemia, familial, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061182"
    ],
    "unlinked_id_list": []
}