Versions

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{
    "count": 1,
    "next": null,
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    "results": [
        {
            "id": 232,
            "hash_id": "553f94c2bb5a1616e5ed459c",
            "name": "Congenital myaesthenic syndrome",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neuromuscular disorders",
            "status": "public",
            "version": "4.5",
            "version_created": "2023-10-25T21:08:55.767856Z",
            "relevant_disorders": [
                "Congenital myaesthenia",
                "Congenital myasthenia",
                "R80"
            ],
            "stats": {
                "number_of_genes": 35,
                "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",
                    "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                },
                {
                    "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."
                }
            ]
        }
    ]
}