{
    "disease_id": "DOID:0110372", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013395", 
            "name": "RHO retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013395", 
            "name": "retinitis pigmentosa, rhodopsin-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013395", 
            "name": "retinitis pigmentosa caused by mutation in RHO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013395", 
            "name": "RP 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013395", 
            "name": "RP4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013395", 
            "name": "retinitis pigmentosa 4; RP4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013395", 
            "name": "retinitis pigmentosa type 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110372", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110372", 
            "name": "RP4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110372", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the RHO gene on chromosome 3q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110372", 
        "name": "retinitis pigmentosa 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110372#disease-associations", 
            "id": "0110372", 
            "database": "Alliance of Genome Resources"
        }
    ]
}