{
    "disease_id": "DOID:0061207",
    "recommended_name": {
        "id": "DOID:0061207",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061207",
        "name": "maple syrup urine disease type II",
        "description": "A maple syrup urine disease that has_material_basis_in homozygous or compound heterozygous mutation in the DBT gene, which encodes a subunit of the branched-chain alpha-keto acid dehydrogenase complex (BCKDC), on chromosome 1p21."
    },
    "synonyms": [
        {
            "id": "MONDO:0023693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023693",
            "name": "maple syrup urine disease type 2",
            "description": "A maple syrup urine disease caused by mutations in DBT."
        },
        {
            "id": "MONDO:0023693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023693",
            "name": "maple syrup urine disease type 2",
            "description": ""
        },
        {
            "id": "MONDO:0023693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023693",
            "name": "MSUD type 2",
            "description": ""
        },
        {
            "id": "MONDO:0023693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023693",
            "name": "MSUD2",
            "description": ""
        },
        {
            "id": "MIM:620699",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620699",
            "name": "Maple syrup urine disease 2",
            "description": "Maple syrup urine disease 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061207"
    ],
    "unlinked_id_list": []
}
