{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012464", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012464", 
            "name": "CORD10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012464", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012464", 
            "name": "cone-Rod dystrophy type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012464", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012464", 
            "name": "SEMA4A cone-rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012464", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012464", 
            "name": "cone-ROD dystrophy 10; CORD10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012464", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012464", 
            "name": "cone-rod dystrophy caused by mutation in SEMA4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111017", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111017", 
            "name": "CORD10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111017", 
        "description": "A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111017", 
        "name": "cone-rod dystrophy 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610283", 
            "id": "610283", 
            "database": "MIM"
        }
    ]
}