{
    "disease_id": "DOID:0110358",
    "recommended_name": {
        "id": "DOID:0110358",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110358",
        "name": "retinitis pigmentosa 12",
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the CRB1 gene on chromosome 1q31.3."
    },
    "synonyms": [
        {
            "id": "DOID:0110358",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110358",
            "name": "RP12",
            "description": ""
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "retinitis pigmentosa 12",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the CRB1 gene."
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "CRB1 retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "RP12",
            "description": ""
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "retinitis pigmentosa 12",
            "description": ""
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "retinitis pigmentosa caused by mutation in CRB1",
            "description": ""
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "retinitis pigmentosa type 12",
            "description": ""
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "retinitis pigmentosa-12",
            "description": ""
        },
        {
            "id": "MONDO:0010818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "name": "RP 12",
            "description": ""
        },
        {
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            "resource": "MIM",
            "url": "https://www.omim.org/entry/600105",
            "name": "Retinitis pigmentosa 12",
            "description": "Retinitis pigmentosa 12"
        }
    ],
    "children": [],
    "id_list": [
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    ],
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        {
            "id": "DOID:0110358",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110358",
            "categories": []
        },
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            "id": "MONDO:0010818",
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            "url": "https://monarchinitiative.org/disease/MONDO:0010818",
            "categories": []
        },
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    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110358"
}
