{
    "disease_id": "DOID:0061205",
    "recommended_name": {
        "id": "DOID:0061205",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061205",
        "name": "mild variant of maple syrup urine disease",
        "description": "A maple syrup urine disease characterized by increased plasma levels of branched-chain amino acids (BCAA) apparent at birth that has_material_basis_in homozygous mutation in the PPM1K gene on chromosome 4q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0014057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014057",
            "name": "maple syrup urine disease, mild variant",
            "description": ""
        },
        {
            "id": "MONDO:0014057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014057",
            "name": "maple syrup urine disease, mild variant",
            "description": ""
        },
        {
            "id": "MONDO:0014057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014057",
            "name": "MSUDMV",
            "description": ""
        },
        {
            "id": "MIM:615135",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615135",
            "name": "Maple syrup urine disease, mild variant",
            "description": "Maple syrup urine disease, mild variant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061205"
    ],
    "unlinked_id_list": []
}