{
    "disease_id": "DOID:0110001",
    "recommended_name": {
        "id": "DOID:0110001",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110001",
        "name": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",
        "description": "A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the SERAC1 gene on chromosome 6q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110001",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110001",
            "name": "3-methylglutaconic aciduria type 6",
            "description": ""
        },
        {
            "id": "DOID:0110001",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110001",
            "name": "MEGDEL",
            "description": ""
        },
        {
            "id": "DOID:0110001",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110001",
            "name": "MEGDEL syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110001",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110001",
            "name": "MGCA6",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",
            "description": "Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene."
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "SERAC1 3-methylglutaconic aciduria",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-MGCA type IV (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "MGCA6",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-MGCA-4 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-Methylglutaconic aciduria, type 6",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-methylglutaconic aciduria caused by mutation in SERAC1",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "MEGDEL",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome; MEGDEL",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-methylglutaconic aciduria type 6",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "MEGDEL syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-methylglutaconic aciduria type VI",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "SERAC1 defect",
            "description": ""
        },
        {
            "id": "MONDO:0013875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013875",
            "name": "3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome",
            "description": ""
        },
        {
            "id": "MIM:614739",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614739",
            "name": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",
            "description": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome"
        }
    ]
}