GET /api/v1/panels/99/versions/?format=api
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 1,
"next": null,
"previous": null,
"results": [
{
"id": 99,
"hash_id": "55e01bb222c1fc6199b42904",
"name": "Haematuria",
"disease_group": "Renal and urinary tract disorders",
"disease_sub_group": "Syndromes with prominent renal abnormalities",
"status": "public",
"version": "2.13",
"version_created": "2023-10-26T01:21:56.491472Z",
"relevant_disorders": [
"Alport syndrome",
"Familial haematuria",
"R194"
],
"stats": {
"number_of_genes": 8,
"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 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."
}
]
}
]
}