{
    "disease_id": "DOID:0111516", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014899", 
            "name": "adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014899", 
            "name": "adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014899", 
            "name": "PEOB4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014899", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014899", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4; PEOB4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014899", 
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014899", 
            "name": "progressive external ophthalmoplegia, autosomal recessive 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111516", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111516", 
            "name": "adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111516", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111516", 
            "name": "PEOB4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111516", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111516", 
            "name": "autosomal recessive progressive external ophthalmoplegia 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111516", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111516", 
            "name": "adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111516", 
        "description": "A chronic progressive external ophthalmoplegia characterized by adult onset of eye muscle weakness and proximal limb muscle weakness that has_material_basis_in homozygous or compound heterozygous mutation in DGUOK on chromosome 2p13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111516", 
        "name": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111516#disease-associations", 
            "id": "0111516", 
            "database": "Alliance of Genome Resources"
        }
    ]
}