{
    "disease_id": "DOID:0061108",
    "recommended_name": {
        "id": "DOID:0061108",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061108",
        "name": "retinitis pigmentosa 79",
        "description": "A retinitis pigmentosa that has_material_basis_in heterozygous mutation in the HK1 gene on chromosome 10q22."
    },
    "synonyms": [
        {
            "id": "DOID:0061108",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061108",
            "name": "RP79",
            "description": ""
        },
        {
            "id": "MONDO:0044320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044320",
            "name": "retinitis pigmentosa 79",
            "description": ""
        },
        {
            "id": "MONDO:0044320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044320",
            "name": "retinitis pigmentosa 79",
            "description": ""
        },
        {
            "id": "MONDO:0044320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044320",
            "name": "RP79",
            "description": ""
        },
        {
            "id": "MIM:617460",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617460",
            "name": "Retinitis pigmentosa 79",
            "description": "Retinitis pigmentosa 79"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061108"
    ],
    "unlinked_id_list": []
}