{
    "disease_id": "DOID:0111521",
    "recommended_name": {
        "id": "DOID:0111521",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111521",
        "name": "autosomal dominant progressive external ophthalmoplegia 1",
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the POLG gene on chromosome 15q26.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111521",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111521",
            "name": "PEOA1",
            "description": ""
        },
        {
            "id": "MONDO:0024528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024528",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1",
            "description": "Any autosomal dominant progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene."
        },
        {
            "id": "MONDO:0024528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024528",
            "name": "PEOA1",
            "description": ""
        },
        {
            "id": "MONDO:0024528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024528",
            "name": "POLG autosomal dominant progressive external ophthalmoplegia",
            "description": ""
        },
        {
            "id": "MONDO:0024528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024528",
            "name": "autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG",
            "description": ""
        },
        {
            "id": "MONDO:0024528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024528",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1",
            "description": ""
        },
        {
            "id": "MONDO:0024528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024528",
            "name": "progressive external ophthalmoplegia, autosomal dominant 1",
            "description": ""
        },
        {
            "id": "MIM:157640",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/157640",
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1",
            "description": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111521"
    ],
    "unlinked_id_list": []
}