{
    "disease_id": "DOID:0070002",
    "recommended_name": {
        "id": "DOID:0070002",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070002",
        "name": "3-methylglutaconic aciduria type 9",
        "description": "A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the TIMM50 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070002",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070002",
            "name": "3-methylglutaconic acuduria type IX, MGCA9",
            "description": ""
        },
        {
            "id": "MONDO:0044724",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044724",
            "name": "3-methylglutaconic aciduria type 9",
            "description": ""
        },
        {
            "id": "MONDO:0044724",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044724",
            "name": "3-methylglutaconic aciduria-epilepsy-spasticity-severe intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0044724",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044724",
            "name": "MGA9",
            "description": ""
        },
        {
            "id": "MONDO:0044724",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044724",
            "name": "MGCA9",
            "description": ""
        },
        {
            "id": "MIM:617698",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617698",
            "name": "3-methylglutaconic aciduria 9",
            "description": "3-methylglutaconic aciduria 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070002"
    ],
    "unlinked_id_list": []
}