{
    "disease_id": "DOID:0111340",
    "recommended_name": {
        "id": "DOID:0111340",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111340",
        "name": "dominant optic atrophy plus syndrome",
        "description": "A syndrome characterized by visual loss and sensorineural hearing loss with onset in childhood and associated with other symptoms including; progressive external ophthalmoplegia, muscle cramps, hyperreflexia, and ataxia that has_material_basis_in heterozygous mutation in the OPA1 gene on chromosome 3q29."
    },
    "synonyms": [
        {
            "id": "DOID:0111340",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111340",
            "name": "DOA+",
            "description": ""
        },
        {
            "id": "DOID:0111340",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111340",
            "name": "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0007429",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007429",
            "name": "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0007429",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007429",
            "name": "optic atrophy plus syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007429",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007429",
            "name": "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0007429",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007429",
            "name": "dominant optic atrophy plus syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007429",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007429",
            "name": "optic atrophy 1 and deafness",
            "description": ""
        },
        {
            "id": "MIM:125250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/125250",
            "name": "Dominant optic atrophy plus syndrome",
            "description": "Dominant optic atrophy plus syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111340"
    ],
    "unlinked_id_list": []
}