{
    "disease_id": "DOID:0111433",
    "recommended_name": {
        "id": "DOID:0111433",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111433",
        "name": "optic atrophy 3",
        "description": "An optic atrophy characterized by optic atrophy and cataract that has_material_basis_in heterozygous mutation in OPA3 on chromosome 19q13.32."
    },
    "synonyms": [
        {
            "id": "DOID:0111433",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111433",
            "name": "ADOAC",
            "description": ""
        },
        {
            "id": "DOID:0111433",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111433",
            "name": "OPA3",
            "description": ""
        },
        {
            "id": "DOID:0111433",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111433",
            "name": "autosomal dominant optic atrophy 3",
            "description": ""
        },
        {
            "id": "DOID:0111433",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111433",
            "name": "autosomal dominant optic atrophy and cataract",
            "description": ""
        },
        {
            "id": "DOID:0111433",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111433",
            "name": "autosomal dominant optic atrophy type 3",
            "description": ""
        },
        {
            "id": "DOID:0111433",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111433",
            "name": "optic atrophy 3 with cataract",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "optic atrophy 3",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "optic atrophy, cataract, and neurologic disorder",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "optic atrophy 3",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "optic atrophy 3, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "optic atrophy 3, autosomal dominant; OPA3",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "autosomal dominant optic atrophy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "OPA3",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "optic atrophy and cataract, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "OPA3, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008133",
            "name": "optic atrophy 3 with cataract",
            "description": ""
        },
        {
            "id": "MIM:165300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/165300",
            "name": "Optic atrophy 3",
            "description": "Optic atrophy 3"
        }
    ]
}