{
    "disease_id": "DOID:11830", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013603", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013603", 
            "name": "MYP20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013603", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013603", 
            "name": "myopia 20, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013603", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013603", 
            "name": "myopia 20, autosomal dominant; MYP20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11830", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11830", 
            "name": "near vision"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11830", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11830", 
            "name": "near-sightedness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11830", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11830", 
            "name": "short-sightedness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11830", 
        "description": "A refractive error characterized by the inability to see farther objects clearly.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11830", 
        "name": "myopia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/11830#disease-associations", 
            "id": "11830", 
            "database": "Alliance of Genome Resources"
        }
    ]
}