{
    "disease_id": "DOID:0080314", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011193", 
            "name": "cone dystrophy 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011193", 
            "name": "GUCA1A cone dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011193", 
            "name": "COD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011193", 
            "name": "cone dystrophy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011193", 
            "name": "cone dystrophy 3; COD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011193", 
            "name": "cone dystrophy caused by mutation in GUCA1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011193", 
            "name": "retinal cone dystrophy"
        }, 
        {
            "url": "https://www.omim.org/entry/602093", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:602093", 
            "name": "Cone dystrophy 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080314", 
        "description": "A cone-rod dystrophy that is characterized by deterioration of the cone in childhood or early adult life and progressive deterioration of the rod photoreceptor cells in later life that has_material_basis_in mutation in GUCA1A on chromosome 6p21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080314", 
        "name": "cone-rod dystrophy 14"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/602093", 
            "id": "602093", 
            "database": "MIM"
        }
    ]
}