{
    "disease_id": "DOID:0111522", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1; PEOB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "autosomal recessive progressive external ophthalmoplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "cerebellar ataxia infantile with progressive external ophthalmoplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "progressive external ophthalmoplegia with cerebellar ataxia infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "POLG autosomal recessive progressive external ophthalmoplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "PEOB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "arPEO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "progressive external ophthalmoplegia, autosomal recessive 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009783", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009783", 
            "name": "autosomal recessive progressive external ophthalmoplegia caused by mutation in POLG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111522", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111522", 
            "name": "PEOB1"
        }, 
        {
            "url": "https://www.omim.org/entry/258450", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:258450", 
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111522", 
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in POLG on chromosome 15q26.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111522", 
        "name": "autosomal recessive progressive external ophthalmoplegia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/258450", 
            "id": "258450", 
            "database": "MIM"
        }
    ]
}