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{
    "count": 1,
    "next": null,
    "previous": null,
    "results": [
        {
            "id": 567,
            "hash_id": null,
            "name": "Adult onset hereditary spastic paraplegia",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "4.1",
            "version_created": "2024-05-01T12:33:35.257005Z",
            "relevant_disorders": [
                "Hereditary spastic paraplegia - adult onset",
                "R60"
            ],
            "stats": {
                "number_of_genes": 107,
                "number_of_strs": 10,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                },
                {
                    "name": "GMS Rare Disease",
                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
                },
                {
                    "name": "GMS signed-off",
                    "slug": "gms-signed-off",
                    "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
                }
            ]
        }
    ]
}