{
    "disease_id": "DOID:0111518", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013117", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013117", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013117", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5; PEOA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013117", 
            "name": "RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013117", 
            "name": "progressive external ophthalmoplegia, autosomal dominant 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013117", 
            "name": "PEOA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013117", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111518", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111518", 
            "name": "autosomal dominant progressive external ophthalmoplegia 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111518", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111518", 
            "name": "PEOA5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111518", 
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in RRM2B on chromosome 8q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111518", 
        "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111518#disease-associations", 
            "id": "0111518", 
            "database": "Alliance of Genome Resources"
        }
    ]
}