GET /api/v1/panels/?page=2
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

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                "Multiple bowel polyps",
                "Peutz-Jeghers syndrome",
                "GI tract",
                "Inherited colorectal cancer (with or without polyposis)"
            ],
            "stats": {
                "number_of_genes": 30,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 249,
            "hash_id": "55507b25bb5a161bf644a3b2",
            "name": "Glaucoma (developmental)",
            "disease_group": "Ophthalmological disorders",
            "disease_sub_group": "Anterior segment abnormalities",
            "status": "public",
            "version": "1.39",
            "version_created": "2021-09-09T10:18:24.656881Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 232,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 528,
            "hash_id": null,
            "name": "Glycogen storage disease",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.7",
            "version_created": "2021-08-26T10:55:47.645321Z",
            "relevant_disorders": [
                "R274"
            ],
            "stats": {
                "number_of_genes": 29,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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": 720,
            "hash_id": null,
            "name": "Groopman et al 2019 - Genes with diagnostic variants",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.8",
            "version_created": "2019-07-09T15:48:14.145108Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 66,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Submitted List",
                    "slug": "submitted-list",
                    "description": "Original list, ratings, comments submitted to PanelApp- generally used for the creation of reference GMS panels, these panels  should be internal only"
                }
            ]
        },
        {
            "id": 473,
            "hash_id": null,
            "name": "Growth failure in early childhood",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.85",
            "version_created": "2021-10-13T16:06:09.294891Z",
            "relevant_disorders": [
                "R147"
            ],
            "stats": {
                "number_of_genes": 153,
                "number_of_strs": 0,
                "number_of_regions": 5
            },
            "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."
                }
            ]
        },
        {
            "id": 59,
            "hash_id": "594a71908f620375d17ea6b2",
            "name": "Haematological malignancies cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "2.21",
            "version_created": "2021-10-13T16:15:23.015932Z",
            "relevant_disorders": [
                "Haemonc",
                "Haematological malignancies pertinent cancer susceptibility"
            ],
            "stats": {
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                "number_of_regions": 0
            },
            "types": [
                {
                    "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": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                },
                {
                    "name": "GMS Cancer Germline Virtual",
                    "slug": "gms-cancer-germline-virtual",
                    "description": "This is a panel used for WGS germline analysis for the GMS."
                }
            ]
        },
        {
            "id": 407,
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            "name": "Haematological malignancies for rare disease",
            "disease_group": "Tumour syndromes",
            "disease_sub_group": "Tumour syndromes",
            "status": "public",
            "version": "1.7",
            "version_created": "2021-10-13T16:15:03.728159Z",
            "relevant_disorders": [],
            "stats": {
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                "number_of_strs": 0,
                "number_of_regions": 0
            },
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                    "name": "Rare Disease 100K",
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                    "description": "Rare Disease 100K"
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            ]
        },
        {
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            "disease_sub_group": "Syndromes with prominent renal abnormalities",
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            "version": "2.11",
            "version_created": "2021-03-10T18:15:28.251141Z",
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                "Familial haematuria",
                "R194"
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                "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": "Rare Disease 100K",
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                    "description": "Rare Disease 100K"
                },
                {
                    "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": 115,
            "hash_id": "596f86a58f620352d0e3eed3",
            "name": "Head and neck cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.057839Z",
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                "Nasopharyngeal",
                "Oral Oropharyngeal",
                "Sinonasal"
            ],
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                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
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            ]
        },
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            "disease_group": "Hearing and ear disorders",
            "disease_sub_group": "Non-syndromic hearing loss",
            "status": "public",
            "version": "2.199",
            "version_created": "2021-10-13T13:44:56.253447Z",
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                "Congenital hearing impairment",
                "Autosomal dominant deafness",
                "Congenital hearing impairment (profound/severe)",
                "R67"
            ],
            "stats": {
                "number_of_genes": 403,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
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                },
                {
                    "name": "GMS Rare Disease Virtual",
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                    "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": "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)"
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            ]
        },
        {
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            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Motor Disorders of the CNS",
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                "number_of_strs": 14,
                "number_of_regions": 3
            },
            "types": [
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                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
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            "name": "Hereditary ataxia - adult onset",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.88",
            "version_created": "2021-10-15T13:39:08.433960Z",
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            },
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                    "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."
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            ]
        },
        {
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            "name": "Hereditary ataxia and cerebellar anomalies - childhood onset",
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            "disease_sub_group": "",
            "status": "public",
            "version": "6.338",
            "version_created": "2021-10-15T10:48:10.574421Z",
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            },
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                    "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."
                },
                {
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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."
                },
                {
                    "name": "Super Panel",
                    "slug": "superpanel",
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            "disease_sub_group": "Anaemias and red cell disorders",
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                "number_of_regions": 0
            },
            "types": [
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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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                {
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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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                "R186"
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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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                    "description": "Rare Disease 100K"
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                {
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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": "Rare Disease 100K"
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        },
        {
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            "name": "Hereditary neuropathy NOT PMP22 copy number",
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            "version": "1.63",
            "version_created": "2021-10-06T12:44:09.644240Z",
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                "Hereditary neuropathy or pain disorder – NOT PMP22 copy number"
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            "stats": {
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            },
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                    "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": "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)"
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        },
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            "disease_sub_group": "Motor Disorders of the CNS",
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            "name": "Hereditary spastic paraplegia - adult onset",
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            "disease_sub_group": "",
            "status": "public",
            "version": "1.73",
            "version_created": "2021-10-15T09:21:58.700705Z",
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                    "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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                    "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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            "name": "Hereditary spastic paraplegia - childhood onset",
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            },
            "types": [
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                    "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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                    "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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            ]
        },
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            "version_created": "2021-09-14T15:35:52.642494Z",
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                "Holoprosencephaly - NOT chromosomal",
                "R85"
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            "stats": {
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                "number_of_regions": 0
            },
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                    "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": "Component Of Super Panel",
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                    "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."
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            ]
        },
        {
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            "disease_group": "Dermatological disorders",
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            "status": "public",
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            "version_created": "2017-11-05T02:37:20.406396Z",
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            "stats": {
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                "number_of_regions": 0
            },
            "types": [
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                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
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            "name": "Hydrocephalus",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.118",
            "version_created": "2021-10-14T12:26:02.096429Z",
            "relevant_disorders": [
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                "R86"
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            "stats": {
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                "number_of_regions": 0
            },
            "types": [
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                    "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."
                },
                {
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            ],
            "stats": {
                "number_of_genes": 9,
                "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": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "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": 112,
            "hash_id": "55928cf522c1fc4f7d26e960",
            "name": "Mitochondrial disorders",
            "disease_group": "Metabolic disorders",
            "disease_sub_group": "Mitochondrial",
            "status": "public",
            "version": "2.54",
            "version_created": "2021-09-30T15:53:53.575623Z",
            "relevant_disorders": [
                "Lactic acidosis",
                "All recognised syndromes and those with suggestive features"
            ],
            "stats": {
                "number_of_genes": 478,
                "number_of_strs": 2,
                "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": "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."
                }
            ]
        },
        {
            "id": 534,
            "hash_id": null,
            "name": "Mitochondrial disorder with complex I deficiency",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.14",
            "version_created": "2021-07-08T10:28:13.875386Z",
            "relevant_disorders": [
                "R353"
            ],
            "stats": {
                "number_of_genes": 51,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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": 535,
            "hash_id": null,
            "name": "Mitochondrial disorder with complex II deficiency",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.3",
            "version_created": "2020-02-17T15:54:32.903706Z",
            "relevant_disorders": [
                "R354"
            ],
            "stats": {
                "number_of_genes": 8,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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."
                }
            ]
        }
    ]
}