{
    "disease_id": "DOID:0111441", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "autosomal dominant optic atrophy, classic form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "optic atrophy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "optic atrophy 1; OPA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "optic atrophy, juvenile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "OAK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "optic atrophy, Kjer type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "OPA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "Kjer optic atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "autosomal dominant optic atrophy, Kjer type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008134", 
            "name": "Kjer-type optic atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111441", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111441", 
            "name": "OPA1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111441", 
        "description": "An optic atrophy characterized by early childhood onset of visual impairment, temporal optic disc pallor, color vision deficits, and centrocecal scotoma of variable density that has_material_basis_in heterozygous mutation in OPA1 on chromosome 3q29.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111441", 
        "name": "optic atrophy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111441#disease-associations", 
            "id": "0111441", 
            "database": "Alliance of Genome Resources"
        }
    ]
}