{
    "disease_id": "DOID:12558", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024528", 
            "name": "progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024528", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1; PEOA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024528", 
            "name": "autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024528", 
            "name": "PEOA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024528", 
            "name": "POLG autosomal dominant progressive external ophthalmoplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024528", 
            "name": "progressive external ophthalmoplegia, autosomal dominant 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12558", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12558", 
            "name": "progressive external ophthalmoplegia"
        }, 
        {
            "url": "https://www.omim.org/entry/157640", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:157640", 
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:12558", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:12558", 
        "name": "chronic progressive external ophthalmoplegia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/157640", 
            "id": "157640", 
            "database": "MIM"
        }
    ]
}