GET /api/v1/panels/307/versions/?format=api
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{
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"results": [
{
"id": 307,
"hash_id": "56e0238b22c1fc09c97a6e46",
"name": "Retinal disorders",
"disease_group": "Ophthalmological disorders",
"disease_sub_group": "Posterior segment abnormalities",
"status": "public",
"version": "5.4",
"version_created": "2024-05-02T13:52:40.847312Z",
"relevant_disorders": [
"Posterior segment abnormalities",
"Cone Dysfunction Syndrome",
"Developmental macular and foveal dystrophy",
"Inherited macular dystrophy",
"Leber Congenital Amaurosis Early-Onset Severe Retinal Dystrophy",
"Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy",
"Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy",
"Rod Dysfunction Syndrome",
"Rod-cone dystrophy",
"Familial exudative vitreoretinopathy",
"Familial exudative retinopathy",
"Sorsby retinal dystrophy",
"Doyne retinal dystrophy",
"R32"
],
"stats": {
"number_of_genes": 422,
"number_of_strs": 1,
"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."
}
]
}
]
}