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