{
    "disease_id": "DOID:0050795", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013129", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013129", 
            "name": "cone dystrophy 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013129", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013129", 
            "name": "PDE6C cone dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013129", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013129", 
            "name": "COD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013129", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013129", 
            "name": "cone dystrophy 4; COD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013129", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013129", 
            "name": "cone dystrophy type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013129", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013129", 
            "name": "cone dystrophy caused by mutation in PDE6C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013129", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013129", 
            "name": "achromatopsia 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050795", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050795", 
            "name": "retinal cone dystrophy"
        }, 
        {
            "url": "https://www.omim.org/entry/613093", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613093", 
            "name": "Cone dystrophy 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050795", 
        "description": "A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050795", 
        "name": "cone dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613093", 
            "id": "613093", 
            "database": "MIM"
        }
    ]
}