{
    "disease_id": "DOID:0111523",
    "recommended_name": {
        "id": "DOID:0111523",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111523",
        "name": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3",
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in TK2 on chromosome 16q21."
    },
    "synonyms": [
        {
            "id": "DOID:0111523",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111523",
            "name": "autosomal recessive progressive external ophthalmoplegia 3",
            "description": ""
        },
        {
            "id": "DOID:0111523",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111523",
            "name": "PEOB3",
            "description": ""
        },
        {
            "id": "MONDO:0014898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014898",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3",
            "description": "Any autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation in the TK2 gene."
        },
        {
            "id": "MONDO:0014898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014898",
            "name": "PEOB3",
            "description": ""
        },
        {
            "id": "MONDO:0014898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014898",
            "name": "TK2 autosomal recessive progressive external ophthalmoplegia",
            "description": ""
        },
        {
            "id": "MONDO:0014898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014898",
            "name": "autosomal recessive progressive external ophthalmoplegia caused by mutation in TK2",
            "description": ""
        },
        {
            "id": "MONDO:0014898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014898",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3",
            "description": ""
        },
        {
            "id": "MONDO:0014898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014898",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3; PEOB3",
            "description": ""
        },
        {
            "id": "MONDO:0014898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014898",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 3",
            "description": ""
        },
        {
            "id": "MIM:617069",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617069",
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3",
            "description": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111523"
    ],
    "unlinked_id_list": []
}