{
    "disease_id": "DOID:0070634",
    "recommended_name": {
        "id": "DOID:0070634",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070634",
        "name": "sitosterolemia 1",
        "description": "A sitosterolemia that has_material_basis_in homozygous or compound heterozygous mutation in the ABCG8 gene on chromosome 2p21."
    },
    "synonyms": [
        {
            "id": "MONDO:0020747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020747",
            "name": "sitosterolemia 1",
            "description": ""
        },
        {
            "id": "MONDO:0020747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020747",
            "name": "STSL1",
            "description": ""
        },
        {
            "id": "MONDO:0020747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020747",
            "name": "sitosterolemia 1",
            "description": ""
        },
        {
            "id": "MIM:210250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/210250",
            "name": "Sitosterolemia 1",
            "description": "Sitosterolemia 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070634"
    ],
    "unlinked_id_list": []
}