{
    "disease_id": "DOID:0111022", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013786", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013786", 
            "name": "CORD16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013786", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013786", 
            "name": "cone-ROD dystrophy 16; CORD16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013786", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013786", 
            "name": "cone-Rod dystrophy type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013786", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013786", 
            "name": "C8orf37 cone-rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013786", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013786", 
            "name": "cone-rod dystrophy caused by mutation in C8orf37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013786", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013786", 
            "name": "retinal dystrophy with early macular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013786", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013786", 
            "name": "retinitis pigmentosa 64"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111022", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111022", 
            "name": "CORD16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111022", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111022", 
            "name": "retinal dystrophy with early macular involvement"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111022", 
        "description": "A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111022", 
        "name": "cone-rod dystrophy 16"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111022#disease-associations", 
            "id": "0111022", 
            "database": "Alliance of Genome Resources"
        }
    ]
}