GET /api/v1/panels/
HTTP 200 OK
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Content-Type: application/json
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{
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            "version_created": "2020-02-18T16:59:14.138222Z",
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                "Adult solid tumours pertinent cancer susceptibility"
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                    "name": "GMS Cancer Germline Virtual",
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                    "description": "This is a panel used for WGS germline analysis for the GMS."
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            "disease_sub_group": "Tumour syndromes",
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            "version_created": "2019-06-20T15:10:02.142139Z",
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            "disease_sub_group": "Skeletal dysplasias",
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                    "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
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            "name": "Amyloidosis",
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                    "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)"
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                    "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
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            "version_created": "2020-02-19T16:00:31.016235Z",
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            "name": "Ataxia and cerebellar anomalies - narrow panel",
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            "version_created": "2020-03-30T13:49:38.830735Z",
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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                    "slug": "research",
                    "description": "This is a gene panel used for research."
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            "disease_sub_group": "Ichthyoses",
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                    "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
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                    "description": "This panel is a component of a Super Panel"
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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                    "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
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            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
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                    "description": "Cancer Germline 100K"
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            "version_created": "2020-03-04T13:53:53.700540Z",
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                    "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."
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                {
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                    "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)"
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                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 7,
            "hash_id": "5763f1d68f620350a22bccdc",
            "name": "Familial dysautonomia",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.8",
            "version_created": "2019-12-13T12:28:55.078886Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 22,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 23,
            "hash_id": "5885e9db8f620309044f8a0a",
            "name": "Familial hidradenitis suppurativa",
            "disease_group": "Dermatological disorders",
            "disease_sub_group": "Skin adnexa disorders",
            "status": "public",
            "version": "1.1",
            "version_created": "2017-11-05T02:37:19.861127Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 11,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 63,
            "hash_id": "58c7f5008f620328d77ce70f",
            "name": "Familial Hirschsprung Disease",
            "disease_group": "Gastroenterological disorders",
            "disease_sub_group": "Gastrointestinal disorders",
            "status": "public",
            "version": "1.6",
            "version_created": "2019-06-20T15:11:10.292595Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 62,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 6,
            "hash_id": "561518be22c1fc212900fb84",
            "name": "Familial hypercholesterolaemia",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Arteriopathies",
            "status": "public",
            "version": "1.26",
            "version_created": "2019-10-07T15:50:14.542064Z",
            "relevant_disorders": [
                "Familial Hypercholesterolaemia",
                "Familial Hypercholesterolemia"
            ],
            "stats": {
                "number_of_genes": 43,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 772,
            "hash_id": null,
            "name": "Familial hypercholesterolaemia - targeted panel",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.3",
            "version_created": "2020-02-17T14:55:48.616957Z",
            "relevant_disorders": [
                "R134"
            ],
            "stats": {
                "number_of_genes": 5,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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."
                }
            ]
        },
        {
            "id": 480,
            "hash_id": null,
            "name": "Familial hyperparathyroidism",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.5",
            "version_created": "2020-03-04T13:48:30.667576Z",
            "relevant_disorders": [
                "R151"
            ],
            "stats": {
                "number_of_genes": 10,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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."
                },
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        }
    ]
}