{
    "disease_id": "DOID:0111433", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "optic atrophy, cataract, and neurologic disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "optic atrophy 3, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "optic atrophy 3, autosomal dominant; OPA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "autosomal dominant optic atrophy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "OPA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "optic atrophy and cataract, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "OPA3, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008133", 
            "name": "optic atrophy 3 with cataract"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111433", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111433", 
            "name": "ADOAC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111433", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111433", 
            "name": "OPA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111433", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111433", 
            "name": "autosomal dominant optic atrophy 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111433", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111433", 
            "name": "autosomal dominant optic atrophy and cataract"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111433", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111433", 
            "name": "autosomal dominant optic atrophy type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111433", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111433", 
            "name": "optic atrophy 3 with cataract"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111433", 
        "description": "An optic atrophy characterized by optic atrophy and cataract that has_material_basis_in heterozygous mutation in OPA3 on chromosome 19q13.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111433", 
        "name": "optic atrophy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111433#disease-associations", 
            "id": "0111433", 
            "database": "Alliance of Genome Resources"
        }
    ]
}