{
    "disease_id": "DOID:0111515", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014656", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014656", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014656", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2; PEOB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014656", 
            "name": "PEOB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014656", 
            "name": "RNASEH1 progressive external ophthalmoplegia with mitochondrial DNA deletions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014656", 
            "name": "progressive external ophthalmoplegia, autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014656", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111515", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111515", 
            "name": "PEOB2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111515", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111515", 
            "name": "adult-onset CPEO with mitochondrial myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111515", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111515", 
            "name": "adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111515", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111515", 
            "name": "autosomal recessive progressive external ophthalmoplegia 2"
        }, 
        {
            "url": "https://www.omim.org/entry/616479", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616479", 
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111515", 
        "description": "A chronic progressive external ophthalmoplegia characterized by adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, and signs and symptoms of spinocerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in RNASEH1 on chromosome 2p25.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111515", 
        "name": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616479", 
            "id": "616479", 
            "database": "MIM"
        }
    ]
}