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