{
    "disease_id": "DOID:0110355", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012363", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012363", 
            "name": "RP32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012363", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012363", 
            "name": "retinitis pigmentosa 32; RP32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012363", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012363", 
            "name": "RP 32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012363", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012363", 
            "name": "retinitis pigmentosa type 32"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110355", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110355", 
            "name": "RP32"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110355", 
        "description": "A retinitis pigmentosa that has_material_basis_in variation in the chromosome region 1p21.3-p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110355", 
        "name": "retinitis pigmentosa 32"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110355#disease-associations", 
            "id": "0110355", 
            "database": "Alliance of Genome Resources"
        }
    ]
}