{
    "disease_id": "DOID:0112141", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112141", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112141", 
            "name": "RP84"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112141", 
        "description": "A retinitis pigmentosa characterized by onset of night blindness between ages 3 and 4 years and complete blindness as early as age 7 that has_material_basis_in homozygous or compound heterozygous mutation in DHX38 on chromosome 16q22.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112141", 
        "name": "retinitis pigmentosa 84"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618220", 
            "id": "618220", 
            "database": "MIM"
        }
    ]
}