{
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            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
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            "description": "", 
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
            "name": "Iraqi-Jewish 'optic atrophy plus'"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
            "name": "optic atrophy plus syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
            "name": "Costeff optic atrophy syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
            "name": "3-alpha methylglutaconic aciduria type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
            "name": "Iraqi Jewish optic atrophy plus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
            "name": "optic atrophy infantile with chorea and spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
            "name": "OPA3 defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009787", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
            "name": "3-methylglutaconic aciduria type III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
            "name": "Costeff optic atrophy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
            "name": "Costeff syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
            "name": "Iraqi-Jewish optic atrophy plus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
            "name": "MGA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110004", 
            "name": "infantile optic atrophy with chorea and spastic paraplegia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110004", 
        "description": "A 3-methylglutaconic aciduria that has_material_basis_in mutation in the OPA3 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110004", 
        "name": "3-methylglutaconic aciduria type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110004#disease-associations", 
            "id": "0110004", 
            "database": "Alliance of Genome Resources"
        }
    ]
}