{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013604", 
            "name": "myopia 21, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013604", 
            "name": "ZNF644 myopia (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013604", 
            "name": "myopia (disease) caused by mutation in ZNF644"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013604", 
            "name": "myopia 21, autosomal dominant; MYP21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013604", 
            "name": "MYP21"
        }, 
        {
            "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"
        }, 
        {
            "url": "https://www.omim.org/entry/614167", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614167", 
            "name": "Myopia 21, autosomal dominant"
        }
    ], 
    "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.omim.org/entry/614167", 
            "id": "614167", 
            "database": "MIM"
        }
    ]
}