GET /api/v1/panels/126/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": 126,
"hash_id": "558ac48fbb5a16630dcfeaad",
"name": "Monogenic hearing loss",
"disease_group": "Hearing and ear disorders",
"disease_sub_group": "Non-syndromic hearing loss",
"status": "public",
"version": "4.41",
"version_created": "2024-05-02T10:13:37.221689Z",
"relevant_disorders": [
"Hearing loss",
"Congenital hearing impairment",
"Autosomal dominant deafness",
"Congenital hearing impairment (profound/severe)",
"Non-syndromic hearing loss",
"R67"
],
"stats": {
"number_of_genes": 422,
"number_of_strs": 0,
"number_of_regions": 1
},
"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": "Component Of Super Panel",
"slug": "component-of-super-panel",
"description": "This panel is a component of a Super Panel"
},
{
"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."
}
]
}
]
}