{
    "disease_id": "DOID:0111340", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007429", 
            "name": "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007429", 
            "name": "optic atrophy 1 and deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111340", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111340", 
            "name": "DOA+"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111340", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111340", 
            "name": "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111340", 
        "description": "A syndrome characterized by visual loss and sensorineural hearing loss with onset in childhood and associated with other symptoms including; progressive external ophthalmoplegia, muscle cramps, hyperreflexia, and ataxia that has_material_basis_in heterozygous mutation in OPA1 on chromosome 3q29.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111340", 
        "name": "dominant optic atrophy plus syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111340#disease-associations", 
            "id": "0111340", 
            "database": "Alliance of Genome Resources"
        }
    ]
}