GET /api/v1/panels/?format=api&page=2
HTTP 200 OK
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Content-Type: application/json
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            "version_created": "2017-11-05T02:37:20.335660Z",
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                "number_of_regions": 0
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                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
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            "version": "1.6",
            "version_created": "2023-10-25T20:41:38.126578Z",
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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 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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            "version_created": "2022-10-10T11:18:50.450537Z",
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                {
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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."
                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
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        },
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        },
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        },
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                {
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        },
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                {
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        },
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                {
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        {
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                {
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        },
        {
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                {
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                {
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        },
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                },
                {
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            ]
        },
        {
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                {
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        },
        {
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        {
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                {
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                {
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                {
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                {
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        },
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            },
            "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": 1341,
            "hash_id": null,
            "name": "GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.1",
            "version_created": "2023-09-14T13:25:34.299435Z",
            "relevant_disorders": [
                "R288"
            ],
            "stats": {
                "number_of_genes": 1,
                "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": "3.87",
            "version_created": "2024-03-26T17:28:05.487139Z",
            "relevant_disorders": [
                "R147"
            ],
            "stats": {
                "number_of_genes": 162,
                "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": "4.4",
            "version_created": "2023-10-25T21:35:42.752028Z",
            "relevant_disorders": [
                "Haemonc",
                "Haematological malignancies pertinent cancer susceptibility"
            ],
            "stats": {
                "number_of_genes": 108,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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."
                },
                {
                    "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": 407,
            "hash_id": null,
            "name": "Haematological malignancies for rare disease",
            "disease_group": "Tumour syndromes",
            "disease_sub_group": "Tumour syndromes",
            "status": "public",
            "version": "1.16",
            "version_created": "2022-11-17T12:00:47.843065Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 89,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 99,
            "hash_id": "55e01bb222c1fc6199b42904",
            "name": "Haematuria",
            "disease_group": "Renal and urinary tract disorders",
            "disease_sub_group": "Syndromes with prominent renal abnormalities",
            "status": "public",
            "version": "2.13",
            "version_created": "2023-10-26T01:21:56.491472Z",
            "relevant_disorders": [
                "Alport syndrome",
                "Familial haematuria",
                "R194"
            ],
            "stats": {
                "number_of_genes": 8,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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."
                },
                {
                    "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."
                }
            ]
        },
        {
            "id": 1342,
            "hash_id": null,
            "name": "Haemoglobinopathy trait or carrier testing",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.7",
            "version_created": "2024-01-05T15:41:53.704086Z",
            "relevant_disorders": [
                "R361"
            ],
            "stats": {
                "number_of_genes": 5,
                "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": 1343,
            "hash_id": null,
            "name": "Haemophagocytic syndrome with absent perforin expression",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.2",
            "version_created": "2023-11-06T15:56:22.916502Z",
            "relevant_disorders": [
                "R232"
            ],
            "stats": {
                "number_of_genes": 1,
                "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": 1344,
            "hash_id": null,
            "name": "Haemophagocytic syndrome with absent XIAP expression",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.1",
            "version_created": "2023-09-14T13:30:03.574365Z",
            "relevant_disorders": [
                "R18"
            ],
            "stats": {
                "number_of_genes": 1,
                "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": 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",
            "relevant_disorders": [
                "Nasopharyngeal",
                "Oral Oropharyngeal",
                "Sinonasal"
            ],
            "stats": {
                "number_of_genes": 12,
                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 1226,
            "hash_id": null,
            "name": "Hereditary alpha tryptasaemia",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.3",
            "version_created": "2023-10-26T10:50:49.247003Z",
            "relevant_disorders": [
                "R436"
            ],
            "stats": {
                "number_of_genes": 1,
                "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": 1345,
            "hash_id": null,
            "name": "Hereditary angioedema types I and II",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.1",
            "version_created": "2023-09-14T13:31:46.646543Z",
            "relevant_disorders": [
                "R341"
            ],
            "stats": {
                "number_of_genes": 1,
                "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": 20,
            "hash_id": "559a7d1022c1fc58ad67fc97",
            "name": "Hereditary ataxia",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Motor Disorders of the CNS",
            "status": "public",
            "version": "1.332",
            "version_created": "2024-01-23T16:09:17.853479Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 167,
                "number_of_strs": 14,
                "number_of_regions": 3
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 488,
            "hash_id": null,
            "name": "Hereditary ataxia and cerebellar anomalies - childhood onset",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "12.95",
            "version_created": "2024-03-18T16:02:36.855301Z",
            "relevant_disorders": [
                "Hereditary ataxia with onset in childhood",
                "Cerebellar anomalies",
                "R55",
                "R84"
            ],
            "stats": {
                "number_of_genes": 477,
                "number_of_strs": 14,
                "number_of_regions": 4
            },
            "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": "Super Panel",
                    "slug": "superpanel",
                    "description": "Superpanel"
                },
                {
                    "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": 466,
            "hash_id": null,
            "name": "Hereditary ataxia with onset in adulthood",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "4.30",
            "version_created": "2024-02-20T14:14:40.400228Z",
            "relevant_disorders": [
                "Hereditary ataxia - adult onset",
                "R54"
            ],
            "stats": {
                "number_of_genes": 247,
                "number_of_strs": 15,
                "number_of_regions": 4
            },
            "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": "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 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."
                }
            ]
        },
        {
            "id": 1221,
            "hash_id": null,
            "name": "Hereditary diffuse gastric cancer",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.1",
            "version_created": "2023-12-20T14:33:31.623245Z",
            "relevant_disorders": [
                "CDH1-related cancer syndrome",
                "R215"
            ],
            "stats": {
                "number_of_genes": 2,
                "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": 157,
            "hash_id": "58c7fba38f6203345887d4f5",
            "name": "Hereditary Erythrocytosis",
            "disease_group": "Haematological disorders",
            "disease_sub_group": "Anaemias and red cell disorders",
            "status": "public",
            "version": "2.6",
            "version_created": "2024-01-24T18:15:31.178499Z",
            "relevant_disorders": [
                "R405"
            ],
            "stats": {
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                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
                    "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": 123,
            "hash_id": "5633857722c1fc582756e3d9",
            "name": "Hereditary haemorrhagic telangiectasia",
            "disease_group": "Respiratory disorders",
            "disease_sub_group": "Vascular lung disorders",
            "status": "public",
            "version": "3.5",
            "version_created": "2023-10-26T01:18:10.174431Z",
            "relevant_disorders": [
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                "R186"
            ],
            "stats": {
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                "number_of_strs": 0,
                "number_of_regions": 0
            },
            "types": [
                {
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                    "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."
                },
                {
                    "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."
                }
            ]
        },
        {
            "id": 1225,
            "hash_id": null,
            "name": "Hereditary isolated diabetes insipidus",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.1",
            "version_created": "2023-12-20T14:35:33.091995Z",
            "relevant_disorders": [
                "Neuropophyseal diabetes insipidus",
                "R440"
            ],
            "stats": {
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                "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": 85,
            "hash_id": "55ad205422c1fc7041340234",
            "name": "Hereditary neuropathy",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Motor and Sensory Disorders of the PNS",
            "status": "public",
            "version": "1.476",
            "version_created": "2024-01-24T11:03:50.239042Z",
            "relevant_disorders": [
                "Charcot-Marie-Tooth disease"
            ],
            "stats": {
                "number_of_genes": 284,
                "number_of_strs": 11,
                "number_of_regions": 2
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 846,
            "hash_id": null,
            "name": "Hereditary neuropathy or pain disorder",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "3.83",
            "version_created": "2024-02-15T17:34:22.027244Z",
            "relevant_disorders": [
                "Hereditary neuropathy NOT PMP22 copy number",
                "Hereditary neuropathy or pain disorder - NOT PMP22 copy number",
                "R78"
            ],
            "stats": {
                "number_of_genes": 310,
                "number_of_strs": 1,
                "number_of_regions": 2
            },
            "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."
                },
                {
                    "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."
                }
            ]
        },
        {
            "id": 165,
            "hash_id": "55ad019f22c1fc7042059038",
            "name": "Hereditary spastic paraplegia",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Motor Disorders of the CNS",
            "status": "public",
            "version": "1.308",
            "version_created": "2023-04-11T11:59:18.515407Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_genes": 115,
                "number_of_strs": 10,
                "number_of_regions": 0
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 502,
            "hash_id": null,
            "name": "Hereditary systemic amyloidosis",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.21",
            "version_created": "2023-10-26T01:25:42.272164Z",
            "relevant_disorders": [
                "Amyloidosis",
                "R204"
            ],
            "stats": {
                "number_of_genes": 11,
                "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."
                },
                {
                    "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."
                }
            ]
        },
        {
            "id": 1346,
            "hash_id": null,
            "name": "Hirschsprung disease",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.1",
            "version_created": "2023-09-14T13:33:11.626937Z",
            "relevant_disorders": [
                "R177"
            ],
            "stats": {
                "number_of_genes": 1,
                "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."
                }
            ]
        }
    ]
}