GET /api/v1/panels/65/versions/?format=api
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 1,
"next": null,
"previous": null,
"results": [
{
"id": 65,
"hash_id": "57ee82ef8f62035c9b2d0487",
"name": "Primary lymphoedema",
"disease_group": "Cardiovascular disorders",
"disease_sub_group": "Lymphatic Disorders",
"status": "public",
"version": "3.11",
"version_created": "2024-04-02T14:27:29.983172Z",
"relevant_disorders": [
"Lymphatic Disorders",
"Meiges disease",
"Meige disease",
"Milroy disease",
"Lymphoedema distichiasis",
"Lipoedema disease",
"R136"
],
"stats": {
"number_of_genes": 57,
"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 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."
}
]
}
]
}