{
    "disease_id": "DOID:0111437", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013069", 
            "name": "autosomal recessive optic atrophy, OPA7 type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013069", 
            "name": "optic atrophy 7 with or without auditory neuropathy; OPA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013069", 
            "name": "optic atrophy 7 with or without auditory neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013069", 
            "name": "OPA7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111437", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111437", 
            "name": "OPA7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111437", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111437", 
            "name": "optic atrophy 7 with or without auditory neuropathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111437", 
        "description": "An optic atrophy characterized by juvenile onset, severe bilateral deficiency in visual acuity, optic disc pallor, and central scotoma that has_material_basis_in homozygous or compound heterozygous mutation in TMEM126A on chromosome 11q14.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111437", 
        "name": "optic atrophy 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111437#disease-associations", 
            "id": "0111437", 
            "database": "Alliance of Genome Resources"
        }
    ]
}