{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012983", 
            "name": "cone-Rod dystrophy type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012983", 
            "name": "cone-ROD dystrophy 12; CORD12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012983", 
            "name": "CORD12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012983", 
            "name": "PROM1 cone-rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012983", 
            "name": "cone-rod dystrophy caused by mutation in PROM1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111019", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111019", 
            "name": "CORD12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111019", 
        "description": "A cone-rod dystrophy that has_material_basis_in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111019", 
        "name": "cone-rod dystrophy 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612657", 
            "id": "612657", 
            "database": "MIM"
        }
    ]
}