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{
"id": 123,
"name": "Hereditary haemorrhagic telangiectasia",
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{
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{
"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."
}
],
"status": "public",
"hash_id": "5633857722c1fc582756e3d9",
"regions": [],
"version": "2.2",
"disease_group": "Respiratory disorders",
"version_created": "2020-03-02T16:56:58.249753Z",
"disease_sub_group": "Vascular lung disorders",
"relevant_disorders": [
"Familial and multiple pulmonary arteriovenous malformations",
"R186"
],
"signed_off": "2020-03-02"
}