GET /api/v1/panels/149/versions/?format=api
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
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{
"count": 1,
"next": null,
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"results": [
{
"id": 149,
"hash_id": "553f94d5bb5a1616e5ed45a5",
"name": "Nephrocalcinosis or nephrolithiasis",
"disease_group": "Renal and urinary tract disorders",
"disease_sub_group": "Disorders of function",
"status": "public",
"version": "4.13",
"version_created": "2024-02-13T16:40:27.008021Z",
"relevant_disorders": [
"Renal tract calcification (or Nephrolithiasis or nephrocalcinosis)",
"Renal tract calcification (or Nephrolithiasis/nephrocalcinosis)",
"R256"
],
"stats": {
"number_of_genes": 51,
"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."
}
]
}
]
}