{
    "disease_id": "DOID:0111024", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014153", 
            "name": "cone-rod dystrophy caused by mutation in RAB28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014153", 
            "name": "cone-ROD dystrophy 18; CORD18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014153", 
            "name": "cone-rod dystrophy type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014153", 
            "name": "CORD18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014153", 
            "name": "RAB28 cone-rod dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111024", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111024", 
            "name": "CORD18"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111024", 
        "description": "A cone-rod dystrophy that has_material_basis_in homozygous mutation in the RAB28 gene on chromosome 4p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111024", 
        "name": "cone-rod dystrophy 18"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615374", 
            "id": "615374", 
            "database": "MIM"
        }
    ]
}