GET /api/v1/panels/568/versions/?format=api
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 1,
"next": null,
"previous": null,
"results": [
{
"id": 568,
"hash_id": null,
"name": "Childhood onset hereditary spastic paraplegia",
"disease_group": "",
"disease_sub_group": "",
"status": "public",
"version": "5.1",
"version_created": "2024-05-01T12:35:05.337658Z",
"relevant_disorders": [
"Hereditary spastic paraplegia - childhood onset",
"R61"
],
"stats": {
"number_of_genes": 149,
"number_of_strs": 10,
"number_of_regions": 1
},
"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 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."
}
]
}
]
}