GET /api/v1/panels/31/versions/?format=api
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 1,
"next": null,
"previous": null,
"results": [
{
"id": 31,
"hash_id": "5763f2938f620350a1996046",
"name": "Congenital hypothyroidism",
"disease_group": "Endocrine disorders",
"disease_sub_group": "Thyroid disorders",
"status": "public",
"version": "2.18",
"version_created": "2023-11-30T12:12:27.487017Z",
"relevant_disorders": [
"Congenital hypothyroidism or thyroid agenesis",
"R145"
],
"stats": {
"number_of_genes": 35,
"number_of_strs": 0,
"number_of_regions": 2
},
"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."
}
]
}
]
}