{
    "disease_id": "DOID:0111519", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "mitochondrial DNA deletion syndrome with progressive myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "mtDNA deletion syndrome with progressive myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6; PEOA6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "mitochondrial DNA deletion syndrome with limb-girdle weakness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "progressive external ophthalmoplegia, autosomal dominant 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "PEOA6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014062", 
            "name": "mtDNA deletion syndrome with limb-girdle weakness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111519", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111519", 
            "name": "autosomal dominant progressive external ophthalmoplegia 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111519", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111519", 
            "name": "mitochondrial DNA deletion syndrome with limb-girdle weakness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111519", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111519", 
            "name": "mitochondrial DNA deletion syndrome with progressive myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111519", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111519", 
            "name": "DNA2-related mitochondrial DNA deletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111519", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111519", 
            "name": "PEOA6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111519", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111519", 
            "name": "mtDNA deletion syndrome with limb-girdle weakness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111519", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111519", 
            "name": "mtDNA deletion syndrome with progressive myopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111519", 
        "description": "A chronic progressive external ophthalmoplegia characterized by muscle weakness, mainly affecting the lower limbs, external ophthalmoplegia, exercise intolerance and mtDNA deletions that has_material_basis_in heterozygous mutation in DNA2 on chromosome 10q21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111519", 
        "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions  6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111519#disease-associations", 
            "id": "0111519", 
            "database": "Alliance of Genome Resources"
        }
    ]
}