{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010969", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010969", 
            "name": "PITPNM3 cone-rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010969", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010969", 
            "name": "cone-ROD dystrophy 5; CORD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010969", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010969", 
            "name": "cone-rod dystrophy caused by mutation in PITPNM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010969", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010969", 
            "name": "cone-rod dystrophy type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010969", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010969", 
            "name": "CORD5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111010", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111010", 
            "name": "CORD5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111010", 
        "description": "A cone-rod dystrophy that has_material_basis_in mutation in the PITPNM3 gene in chromosome region 17p13.2-p13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111010", 
        "name": "cone-rod dystrophy 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600977", 
            "id": "600977", 
            "database": "MIM"
        }
    ]
}