{
    "disease_id": "DOID:0111005",
    "recommended_name": {
        "id": "DOID:0111005",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111005",
        "name": "cone-rod dystrophy 2",
        "description": "A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0111005",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111005",
            "name": "CORD2",
            "description": ""
        },
        {
            "id": "DOID:0111005",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111005",
            "name": "CRD2",
            "description": ""
        },
        {
            "id": "DOID:0111005",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111005",
            "name": "RCRD2",
            "description": ""
        },
        {
            "id": "DOID:0111005",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111005",
            "name": "cone-rod retinal dystrophy 2",
            "description": ""
        },
        {
            "id": "DOID:0111005",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111005",
            "name": "retinal cone-rod dystrophy 2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod dystrophy 2",
            "description": "Any cone-rod dystrophy in which the cause of the disease is a mutation in the CRX gene."
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "CORD2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "CRD2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "CRX cone-rod dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "RCRD2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod dystrophy 2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod dystrophy caused by mutation in CRX",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod dystrophy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod retinal dystrophy 2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod retinal dystrophy-2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "retinal cone-rod dystrophy 2",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "cone-rod retinal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007362",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007362",
            "name": "retinal cone-rod dystrophy",
            "description": ""
        },
        {
            "id": "MIM:120970",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/120970",
            "name": "Cone-rod dystrophy 2",
            "description": "Cone-rod dystrophy 2"
        }
    ]
}