{
    "disease_id": "DOID:0111022",
    "recommended_name": {
        "id": "DOID:0111022",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111022",
        "name": "cone-rod dystrophy 16",
        "description": "A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22."
    },
    "synonyms": [
        {
            "id": "DOID:0111022",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111022",
            "name": "CORD16",
            "description": ""
        },
        {
            "id": "DOID:0111022",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111022",
            "name": "retinal dystrophy with early macular involvement",
            "description": ""
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "cone-rod dystrophy 16",
            "description": "Any cone-rod dystrophy in which the cause of the disease is a mutation in the C8orf37 gene."
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "C8orf37 cone-rod dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "CORD16",
            "description": ""
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "cone-rod dystrophy 16",
            "description": ""
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "cone-rod dystrophy caused by mutation in C8orf37",
            "description": ""
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "cone-rod dystrophy type 16",
            "description": ""
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "retinal dystrophy with early macular involvement",
            "description": ""
        },
        {
            "id": "MONDO:0013786",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013786",
            "name": "retinitis pigmentosa 64",
            "description": ""
        },
        {
            "id": "MIM:614500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614500",
            "name": "Cone-rod dystrophy 16",
            "description": "Cone-rod dystrophy 16"
        }
    ]
}