{
    "disease_id": "DOID:0110414", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "RP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "cone-Rod Degeneration, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "retinitis pigmentosa 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "retinitis pigmentosa type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "retinitis pigmentosa caused by mutation in RPGR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "RPGR retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "retinitis pigmentosa 3; RP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010227", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010227", 
            "name": "Choroidoretinal Degeneration with retinal reflex in heterozygous Women"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110414", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110414", 
            "name": "RP3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110414", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the RPGR gene on chromosome Xp11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110414", 
        "name": "retinitis pigmentosa 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110414#disease-associations", 
            "id": "0110414", 
            "database": "Alliance of Genome Resources"
        }
    ]
}