{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014256", 
            "name": "retinitis pigmentosa caused by mutation in NEK2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014256", 
            "name": "retinitis pigmentosa type 67"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014256", 
            "name": "retinitis pigmentosa 67; RP67"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014256", 
            "name": "NEK2 retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014256", 
            "name": "RP67"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110359", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110359", 
            "name": "RP67"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110359", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the NEK2 gene on chromosome 1q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110359", 
        "name": "retinitis pigmentosa 67"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615565", 
            "id": "615565", 
            "database": "MIM"
        }
    ]
}