{
    "disease_id": "DOID:0112140", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112140", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112140", 
            "name": "RP83"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112140", 
        "description": "A retinitis pigmentosa characterized by onset of night blindness in the first decade of life, decreased central vision in the second decade of life, and retinal degeneration that has_material_basis_in heterozygous mutation in ARL3 on chromosome 10q24.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112140", 
        "name": "retinitis pigmentosa 83"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618173", 
            "id": "618173", 
            "database": "MIM"
        }
    ]
}