{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012415", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012415", 
            "name": "progressive external ophthalmoplegia, autosomal dominant 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012415", 
            "name": "POLG2 progressive external ophthalmoplegia with mitochondrial DNA deletions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012415", 
            "name": "PEOA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012415", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in POLG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012415", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012415", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4; PEOA4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111525", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111525", 
            "name": "autosomal dominant progressive external ophthalmoplegia 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111525", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111525", 
            "name": "PEOA4"
        }, 
        {
            "url": "https://www.omim.org/entry/610131", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610131", 
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111525", 
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in POLG2 on chromosome 17q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111525", 
        "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610131", 
            "id": "610131", 
            "database": "MIM"
        }
    ]
}