{
    "disease_id": "DOID:12934", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "Kearns-Sayre syndrome; KSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "KSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "CPEO with ragged-Red fibers"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "ophthalmoplegia, pigmentary Degeneration of retina, and cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "CPEO with ragged red fibers"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "chronic progressive external ophthalmoplegia with myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "CPEO with myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "ophthalmoplegia, progressive external, with ragged-Red fibers"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "ophthalmoplegia plus syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "ophthalmoplegia, progressive external, with ragged red fibers"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "mitochondrial Cytopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "oculocraniosomatic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010787", 
            "name": "ophthalmoplegia-plus syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:12934", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:12934", 
        "name": "Kearns-Sayre syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/12934#disease-associations", 
            "id": "12934", 
            "database": "Alliance of Genome Resources"
        }
    ]
}