{
    "disease_id": "DOID:0111005", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "cone-ROD dystrophy 2; CORD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "CORD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "cone-rod dystrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "RCRD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "cone-rod retinal dystrophy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "CRD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "cone-Rod retinal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "CRX cone-rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "retinal cone-rod dystrophy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "cone-Rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "retinal cone-Rod dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007362", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007362", 
            "name": "cone-rod dystrophy caused by mutation in CRX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111005", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111005", 
            "name": "CORD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111005", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111005", 
            "name": "CRD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111005", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111005", 
            "name": "RCRD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111005", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111005", 
            "name": "cone-rod retinal dystrophy 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111005", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111005", 
            "name": "retinal cone-rod dystrophy 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111005", 
        "description": "A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111005", 
        "name": "cone-rod dystrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/120970", 
            "id": "120970", 
            "database": "MIM"
        }
    ]
}