{
    "disease_id": "DOID:0111436", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015011", 
            "name": "OPA11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015011", 
            "name": "YME1L1 autosomal recessive isolated optic atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015011", 
            "name": "optic atrophy type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015011", 
            "name": "autosomal recessive isolated optic atrophy caused by mutation in YME1L1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111436", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111436", 
            "name": "OPA11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111436", 
        "description": "An optic atrophy characterized by delayed psychomotor development, intellectual disability, ataxia, optic atrophy, and leukoencephalopathy consistent with mitochondrial dysfunction that has_material_basis_in homozygous or compound heterozygous mutation in YME1L1 on chromosome 10p12.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111436", 
        "name": "optic atrophy 11"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617302", 
            "id": "617302", 
            "database": "MIM"
        }
    ]
}