{
    "disease_id": "DOID:0110405",
    "recommended_name": {
        "id": "DOID:0110405",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110405",
        "name": "retinitis pigmentosa 36",
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the PRCD gene on chromosome 17q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110405",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110405",
            "name": "RP36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa 36",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRCD gene."
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "PRCD retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "RP36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa 36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa caused by mutation in PRCD",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa type 36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "RP 36",
            "description": ""
        },
        {
            "id": "MIM:610599",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610599",
            "name": "Retinitis pigmentosa 36",
            "description": "Retinitis pigmentosa 36"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110405"
    ],
    "unlinked_id_list": []
}