{
    "disease_id": "DOID:0111440",
    "recommended_name": {
        "id": "DOID:0111440",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111440",
        "name": "optic atrophy 4",
        "description": "An optic atrophy that has_material_basis_in heterozygous mutation in a region on chromosome 18q12.2-q12.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111440",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111440",
            "name": "OPA4",
            "description": ""
        },
        {
            "id": "MONDO:0011536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011536",
            "name": "optic atrophy 4",
            "description": ""
        },
        {
            "id": "MONDO:0011536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011536",
            "name": "optic atrophy 4",
            "description": ""
        },
        {
            "id": "MONDO:0011536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011536",
            "name": "optic atrophy 4; OPA4",
            "description": ""
        },
        {
            "id": "MONDO:0011536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011536",
            "name": "OPA4",
            "description": ""
        }
    ]
}