{
    "disease_id": "DOID:0111011", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011143", 
            "name": "cone-ROD dystrophy 6; CORD6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011143", 
            "name": "RCD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011143", 
            "name": "cone-rod dystrophy caused by mutation in GUCY2D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011143", 
            "name": "cone-Rod dystrophy type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011143", 
            "name": "GUCY2D cone-rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011143", 
            "name": "retinal cone dystrophy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011143", 
            "name": "CORD6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111011", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111011", 
            "name": "CORD6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111011", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111011", 
            "name": "RCD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111011", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111011", 
            "name": "retinal cone dystrophy 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111011", 
        "description": "A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111011", 
        "name": "cone-rod dystrophy 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111011#disease-associations", 
            "id": "0111011", 
            "database": "Alliance of Genome Resources"
        }
    ]
}