{
    "disease_id": "DOID:0111435",
    "recommended_name": {
        "id": "DOID:0111435",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111435",
        "name": "optic atrophy 6",
        "description": "An optic atrophy characterized by early onset of slowly progressive isolated optic atrophy that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 8q21-q22."
    },
    "synonyms": [
        {
            "id": "DOID:0111435",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111435",
            "name": "OPA6",
            "description": ""
        },
        {
            "id": "MONDO:0009786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009786",
            "name": "optic atrophy 6",
            "description": ""
        },
        {
            "id": "MONDO:0009786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009786",
            "name": "optic atrophy 6",
            "description": ""
        },
        {
            "id": "MONDO:0009786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009786",
            "name": "OPA6",
            "description": ""
        },
        {
            "id": "MONDO:0009786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009786",
            "name": "optic atrophy, congenital or early infantile, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009786",
            "name": "optic atrophy 6; OPA6",
            "description": ""
        }
    ]
}