{
    "disease_id": "DOID:0050476", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "X-linked cardioskeletal myopathy and neutropenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "Mga, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "3-methylglutaconic aciduria type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "cardioskeletal myopathy with neutropenia and abnormal mitochondria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "TAZ defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "BTHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "MGA type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "cardioskeletal myopathy-neutropenia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "3-methylglutaconic aciduria type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "3-Methylglutaconicaciduria type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "MGA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "3-Methylglutaconicaciduria type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "BARTH syndrome; BTHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "MGA type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010543", 
            "name": "3-Methylglutaconic aciduria, type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050476", 
            "name": "3-methylglutaconicaciduria type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050476", 
            "name": "3-methylglutaconicaciduria type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050476", 
            "name": "MGA Type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050476", 
            "name": "MGA type II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050476", 
        "description": "A lipid metabolism disorder that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050476", 
        "name": "Barth syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050476#disease-associations", 
            "id": "0050476", 
            "database": "Alliance of Genome Resources"
        }
    ]
}