{
    "disease_id": "DOID:0110002", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-METHYLGLUTACONIC aciduria, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-Methylglutaconic aciduria, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-Mg-Coa-hydratase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3 methylglutaconyl CoA hydratase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-methylglutaconic aciduria caused by mutation in AUH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3 alpha methylglutaconic aciduria type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "MGA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "Mga, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-MGCA type I (3-MGCA-1)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "MGCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-METHYLGLUTACONIC aciduria, type I; MGCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "MGA type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "AUH 3-methylglutaconic aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3MG-CoA hydratase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3MG CoA hydratase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-methylglutaconyl-CoA hydratase deficiency (auh defect)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-methylglutaconic aciduria type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3-methylglutaconyl-Coa hydratase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009610", 
            "name": "3 methylglutaconic aciduria type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110002", 
            "name": "3-methylglutaconic aciduria type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110002", 
            "name": "3-methylglutaconyl-CoA hydratase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110002", 
            "name": "3MG-CoA hydratase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110002", 
            "name": "MGA type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110002", 
            "name": "MGA1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110002", 
        "description": "A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110002", 
        "name": "3-methylglutaconic aciduria type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110002#disease-associations", 
            "id": "0110002", 
            "database": "Alliance of Genome Resources"
        }
    ]
}