{
    "disease_id": "DOID:0080350", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015013", 
            "name": "retinitis pigmentosa caused by mutation in REEP6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015013", 
            "name": "retinitis pigmentosa type 77"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015013", 
            "name": "REEP6 retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015013", 
            "name": "RP77"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080350", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the REEP6 gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080350", 
        "name": "retinitis pigmentosa 77"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080350#disease-associations", 
            "id": "0080350", 
            "database": "Alliance of Genome Resources"
        }
    ]
}