Versions

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{
    "count": 1,
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    "results": [
        {
            "id": 230,
            "hash_id": "553f979fbb5a1616e5ed45f8",
            "name": "Bilateral congenital or childhood onset cataracts",
            "disease_group": "Ophthalmological disorders",
            "disease_sub_group": "Anterior segment abnormalities",
            "status": "public",
            "version": "4.14",
            "version_created": "2024-05-02T13:25:01.094320Z",
            "relevant_disorders": [
                "Cataracts",
                "R31"
            ],
            "stats": {
                "number_of_genes": 201,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "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 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."
                }
            ]
        }
    ]
}