{
    "disease_id": "DOID:0110397", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013402", 
            "name": "RP27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013402", 
            "name": "NRL retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013402", 
            "name": "retinitis pigmentosa type 27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013402", 
            "name": "retinitis pigmentosa caused by mutation in NRL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013402", 
            "name": "retinal Degeneration, autosomal recessive, Clumped pigment type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013402", 
            "name": "retinitis pigmentosa 27; RP27"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110397", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110397", 
            "name": "RP27"
        }, 
        {
            "url": "https://www.omim.org/entry/613750", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613750", 
            "name": "Retinal degeneration autosomal recessive clumped pigment type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110397", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the NRL gene on chromosome 14q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110397", 
        "name": "retinitis pigmentosa 27"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613750", 
            "id": "613750", 
            "database": "MIM"
        }
    ]
}