{
    "disease_id": "DOID:0110372",
    "recommended_name": {
        "id": "DOID:0110372",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110372",
        "name": "retinitis pigmentosa 4",
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the RHO gene on chromosome 3q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110372",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110372",
            "name": "RP4",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "retinitis pigmentosa 4",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the RHO gene."
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "RHO retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "RP4",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "retinitis pigmentosa 4",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "retinitis pigmentosa 4, autosomal dominant or recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "retinitis pigmentosa caused by mutation in RHO",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "retinitis pigmentosa type 4",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "RP 4",
            "description": ""
        },
        {
            "id": "MONDO:0013395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013395",
            "name": "retinitis pigmentosa, rhodopsin-related",
            "description": ""
        },
        {
            "id": "MIM:613731",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613731",
            "name": "Retinitis pigmentosa 4",
            "description": "Retinitis pigmentosa 4"
        }
    ]
}