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