{
    "disease_id": "DOID:0111524",
    "recommended_name": {
        "id": "DOID:0111524",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111524",
        "name": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5",
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the TOP3A gene on chromosome 17p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111524",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111524",
            "name": "PEOB5",
            "description": ""
        },
        {
            "id": "DOID:0111524",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111524",
            "name": "autosomal recessive progressive external ophthalmoplegia 5",
            "description": ""
        },
        {
            "id": "MONDO:0020845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020845",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5",
            "description": ""
        },
        {
            "id": "MONDO:0020845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020845",
            "name": "PEOB5",
            "description": ""
        },
        {
            "id": "MONDO:0020845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020845",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5",
            "description": ""
        },
        {
            "id": "MONDO:0020845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020845",
            "name": "progressive external ophthalmoplegia, autosomal recessive 5",
            "description": ""
        },
        {
            "id": "MIM:618098",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618098",
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5",
            "description": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111524"
    ],
    "unlinked_id_list": []
}