{
    "disease_id": "DOID:0111520", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012241", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012241", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012241", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3; PEOA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012241", 
            "name": "progressive external ophthalmoplegia, autosomal dominant 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012241", 
            "name": "TWNK progressive external ophthalmoplegia with mitochondrial DNA deletions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012241", 
            "name": "PEOA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012241", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in TWNK"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111520", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111520", 
            "name": "PEOA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111520", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111520", 
            "name": "autosomal dominant progressive external ophthalmoplegia 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111520", 
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in TWNK on chromosome 10q24.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111520", 
        "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111520#disease-associations", 
            "id": "0111520", 
            "database": "Alliance of Genome Resources"
        }
    ]
}