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

{
    "count": 298,
    "next": "https://panelapp.genomicsengland.co.uk/api/v1/panels/?page=2",
    "previous": null,
    "results": [
        {
            "id": 540,
            "hash_id": null,
            "name": "Adult onset movement disorder",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.43",
            "version_created": "2019-01-11T16:25:35.145010Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 11,
                "number_of_genes": 194
            },
            "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)"
                }
            ]
        },
        {
            "id": 391,
            "hash_id": null,
            "name": "Adult solid tumours for rare disease",
            "disease_group": "Tumour syndromes",
            "disease_sub_group": "Tumour syndromes",
            "status": "public",
            "version": "1.21",
            "version_created": "2018-12-11T12:56:38.497201Z",
            "relevant_disorders": [
                "Young adult onset cancer",
                "Exceptionally young adult onset cancer",
                "Multiple Tumours",
                "Rare tumour predisposition syndromes"
            ],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 58
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 245,
            "hash_id": "595ce30f8f62036352471f39",
            "name": "Adult solid tumours pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.292234Z",
            "relevant_disorders": [
                "Carcinoma of unknown primary",
                "Other"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 54
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 511,
            "hash_id": null,
            "name": "Albinism or congenital nystagmus",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.13",
            "version_created": "2019-02-13T12:10:56.746304Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 31
            },
            "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)"
                }
            ]
        },
        {
            "id": 269,
            "hash_id": "58c7f3c78f620328d77ce70e",
            "name": "Amelogenesis imperfecta",
            "disease_group": "Skeletal disorders",
            "disease_sub_group": "Skeletal dysplasias",
            "status": "public",
            "version": "1.7",
            "version_created": "2018-12-17T09:55:36.360380Z",
            "relevant_disorders": [
                "Amelogenesis Imperfecta"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 39
            },
            "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)"
                }
            ]
        },
        {
            "id": 502,
            "hash_id": null,
            "name": "Amyloidosis",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.4",
            "version_created": "2019-02-02T15:49:34.689702Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 10
            },
            "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)"
                }
            ]
        },
        {
            "id": 263,
            "hash_id": "55d30b0322c1fc2ff2a5bf7b",
            "name": "Amyotrophic lateral sclerosis/motor neuron disease",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neurodegenerative disorders",
            "status": "public",
            "version": "1.26",
            "version_created": "2018-12-07T11:43:08.799661Z",
            "relevant_disorders": [
                "Amyotrophic lateral sclerosis or motor neuron disease"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 4,
                "number_of_genes": 30
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 510,
            "hash_id": null,
            "name": "Aniridia",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.0",
            "version_created": "2019-01-28T10:43:36.827266Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 3
            },
            "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)"
                }
            ]
        },
        {
            "id": 34,
            "hash_id": "553f97abbb5a1616e5ed45f9",
            "name": "Anophthalmia or microphthalmia",
            "disease_group": "Ophthalmological disorders",
            "disease_sub_group": "Ocular malformations",
            "status": "public",
            "version": "1.17",
            "version_created": "2019-02-15T11:47:13.583658Z",
            "relevant_disorders": [
                "Anophthalmia or microphthamia",
                "Anophthalmia/microphthamia",
                "Anophthalmia/microphthalmia"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 57
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 134,
            "hash_id": "55a3876e22c1fc63fec6d0da",
            "name": "Arrhythmogenic cardiomyopathy",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Cardiomyopathy",
            "status": "public",
            "version": "1.20",
            "version_created": "2019-02-21T17:05:27.516708Z",
            "relevant_disorders": [
                "Arrhythmogenic Right Ventricular Cardiomyopathy",
                "Arrythmogenic cardiomyopathy"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 18
            },
            "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)"
                }
            ]
        },
        {
            "id": 258,
            "hash_id": "55b75d5b22c1fc05fd2345c9",
            "name": "Arthrogryposis",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neuromuscular disorders",
            "status": "public",
            "version": "2.37",
            "version_created": "2019-01-08T17:28:10.298059Z",
            "relevant_disorders": [
                "Arthrogrythsis"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 245
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 497,
            "hash_id": null,
            "name": "Arthrogryposis - broad panel",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.2",
            "version_created": "2019-02-01T14:36:13.374152Z",
            "relevant_disorders": [
                "Arthrogryposis"
            ],
            "stats": {
                "number_of_regions": 5,
                "number_of_strs": 2,
                "number_of_genes": 489
            },
            "types": [
                {
                    "name": "Super Panel",
                    "slug": "superpanel",
                    "description": "Superpanel"
                },
                {
                    "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": 477,
            "hash_id": null,
            "name": "Ataxia and cerebellar anomalies - narrow panel",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.0",
            "version_created": "2019-01-09T17:56:16.609787Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 3,
                "number_of_strs": 13,
                "number_of_genes": 196
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 139,
            "hash_id": "563248da22c1fc58285b283a",
            "name": "Atypical haemolytic uraemic syndrome",
            "disease_group": "Renal and urinary tract disorders",
            "disease_sub_group": "Syndromes with prominent renal abnormalities",
            "status": "public",
            "version": "1.7",
            "version_created": "2019-02-12T12:40:42.563719Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 13
            },
            "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)"
                }
            ]
        },
        {
            "id": 260,
            "hash_id": "55b20bdf22c1fc7dd6b9bbb7",
            "name": "Auditory Neuropathy Spectrum Disorde",
            "disease_group": "Hearing and ear disorders",
            "disease_sub_group": "Non-syndromic hearing loss",
            "status": "public",
            "version": "1.8",
            "version_created": "2019-02-17T23:29:21.469051Z",
            "relevant_disorders": [
                "Auditory Neuropathy Spectrum Disorder",
                "Auditory Neuropathy Spectrum Disorde"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 5
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 282,
            "hash_id": "562e5d2622c1fc582756e3b5",
            "name": "Autosomal recessive congenital ichthyosis",
            "disease_group": "Dermatological disorders",
            "disease_sub_group": "Ichthyoses",
            "status": "public",
            "version": "1.7",
            "version_created": "2017-11-05T02:37:20.354821Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 14
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 557,
            "hash_id": null,
            "name": "Autosomal recessive primary hypertrophic osteoarthropathy",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.7",
            "version_created": "2019-02-18T14:20:35.976784Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 543,
            "hash_id": null,
            "name": "Bardet Biedl syndrome",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.19",
            "version_created": "2019-03-15T13:35:36.713401Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 24
            },
            "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)"
                }
            ]
        },
        {
            "id": 38,
            "hash_id": "56fa8eb88f62030f36e3026b",
            "name": "Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders",
            "disease_group": "Growth disorders",
            "disease_sub_group": "Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders",
            "status": "public",
            "version": "1.44",
            "version_created": "2019-03-18T11:57:19.373035Z",
            "relevant_disorders": [
                "Atypical Beckwith-Wiedemann syndrome",
                "Classical Beckwith-Wiedemann syndrome",
                "Simpson-Golabi-Behmel syndrome",
                "Sotos syndrome",
                "Weaver syndrome"
            ],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 20
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 208,
            "hash_id": "596f48578f620352d12240e4",
            "name": "Bladder cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.228385Z",
            "relevant_disorders": [
                "Bladder"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 4
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 545,
            "hash_id": null,
            "name": "Bleeding and platelet disorders",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.52",
            "version_created": "2019-03-18T16:04:37.052127Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 110
            },
            "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)"
                }
            ]
        },
        {
            "id": 166,
            "hash_id": "596f81208f620352d0e3eea7",
            "name": "Brain cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.153599Z",
            "relevant_disorders": [
                "Adult Glioma"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 7
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 90,
            "hash_id": "55c2321822c1fc0fe5e416e1",
            "name": "Brain channelopathy",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Channelopathies",
            "status": "public",
            "version": "1.52",
            "version_created": "2019-01-09T13:43:39.338221Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 5,
                "number_of_genes": 24
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 55,
            "hash_id": "596f82e88f620352d0e3eeb1",
            "name": "Breast cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:19.933392Z",
            "relevant_disorders": [
                "Breast"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 5
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 13,
            "hash_id": "55a3a78122c1fc6711b0c6b5",
            "name": "Brugada syndrome",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Cardiac arrhythmia",
            "status": "public",
            "version": "1.35",
            "version_created": "2019-03-01T17:27:09.997606Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 23
            },
            "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)"
                }
            ]
        },
        {
            "id": 234,
            "hash_id": "553f9696bb5a1616e5ed45d1",
            "name": "CAKUT",
            "disease_group": "Renal and urinary tract disorders",
            "disease_sub_group": "Structural renal and urinary tract disease",
            "status": "public",
            "version": "1.34",
            "version_created": "2019-01-30T15:05:14.897132Z",
            "relevant_disorders": [
                "Congenital Anomaly of the Kidneys and Urinary Tract (CAKUT)"
            ],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 65
            },
            "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."
                }
            ]
        },
        {
            "id": 468,
            "hash_id": null,
            "name": "Cardiac arrhythmias",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.0",
            "version_created": "2019-01-28T10:44:49.224543Z",
            "relevant_disorders": [
                "Cardiac arrythmias"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 43
            },
            "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."
                }
            ]
        },
        {
            "id": 469,
            "hash_id": null,
            "name": "Cardiomyopathies - including childhood onset",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.5",
            "version_created": "2019-03-08T17:03:55.967808Z",
            "relevant_disorders": [
                "Paediatric or syndromic cardiomyopathy"
            ],
            "stats": {
                "number_of_regions": 2,
                "number_of_strs": 2,
                "number_of_genes": 993
            },
            "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 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": 230,
            "hash_id": "553f979fbb5a1616e5ed45f8",
            "name": "Cataracts",
            "disease_group": "Ophthalmological disorders",
            "disease_sub_group": "Anterior segment abnormalities",
            "status": "public",
            "version": "1.26",
            "version_created": "2019-02-19T10:51:30.380661Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 157
            },
            "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."
                }
            ]
        },
        {
            "id": 214,
            "hash_id": "55a3aac122c1fc6710839b7d",
            "name": "Catecholaminergic polymorphic VT",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Cardiac arrhythmia",
            "status": "public",
            "version": "1.10",
            "version_created": "2019-03-04T21:13:38.599794Z",
            "relevant_disorders": [
                "Catecholaminergic Polymorphic Ventricular Tachycardia"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 10
            },
            "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)"
                }
            ]
        },
        {
            "id": 286,
            "hash_id": "568f871422c1fc1c79ca176d",
            "name": "Cerebellar hypoplasia",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Motor Disorders of the CNS",
            "status": "public",
            "version": "1.33",
            "version_created": "2019-03-12T12:14:57.224578Z",
            "relevant_disorders": [
                "Cerebellar Hypoplasia",
                "Pontine tegmental cap dysplasia"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 65
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 109,
            "hash_id": "55537918bb5a161bf644a3c7",
            "name": "Cerebral folate deficiency",
            "disease_group": "Metabolic disorders",
            "disease_sub_group": "Specific metabolic abnormalities",
            "status": "public",
            "version": "1.2",
            "version_created": "2017-11-05T02:37:20.047324Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 4
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 491,
            "hash_id": null,
            "name": "Cerebral malformations",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.5",
            "version_created": "2019-03-12T12:14:40.416022Z",
            "relevant_disorders": [
                "Cerebral malformation"
            ],
            "stats": {
                "number_of_regions": 6,
                "number_of_strs": 13,
                "number_of_genes": 596
            },
            "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"
                }
            ]
        },
        {
            "id": 147,
            "hash_id": "5819a24f8f6203341de99c89",
            "name": "Cerebral vascular malformations",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Cerebrovascular disorders",
            "status": "public",
            "version": "1.36",
            "version_created": "2018-12-16T17:21:50.776136Z",
            "relevant_disorders": [
                "Cerebrovascular disorders",
                "Vein of Galen malformation",
                "Cerebral arteriovenous malformations",
                "Moyamoya disease"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 93
            },
            "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."
                }
            ]
        },
        {
            "id": 259,
            "hash_id": "595cd7cc8f62036352471ea1",
            "name": "Childhood solid tumours pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.315247Z",
            "relevant_disorders": [
                "Childhood"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 71
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 221,
            "hash_id": "553f9697bb5a1616e5ed45d3",
            "name": "Choanal atresia",
            "disease_group": "Skeletal disorders",
            "disease_sub_group": "Choanal anomalies",
            "status": "public",
            "version": "1.12",
            "version_created": "2017-11-05T02:37:20.252051Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 12
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 544,
            "hash_id": null,
            "name": "Cholestasis",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.22",
            "version_created": "2019-02-04T11:23:49.198034Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 39
            },
            "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)"
                }
            ]
        },
        {
            "id": 30,
            "hash_id": "554a0ac9bb5a167e4ccd1ec0",
            "name": "Chondrodysplasia punctata",
            "disease_group": "Skeletal disorders",
            "disease_sub_group": "Skeletal dysplasias",
            "status": "public",
            "version": "1.2",
            "version_created": "2017-11-05T02:37:19.878296Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 5
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 197,
            "hash_id": "553f968cbb5a1616e5ed45cc",
            "name": "Classical tuberous sclerosis",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neurodevelopmental disorders",
            "status": "public",
            "version": "1.2",
            "version_created": "2017-11-05T02:37:20.208587Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 2
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 81,
            "hash_id": "57acb8268f620364dc61afd3",
            "name": "Clefting",
            "disease_group": "Dysmorphic and congenital abnormality syndromes",
            "disease_sub_group": "Dysmorphic disorders",
            "status": "public",
            "version": "1.34",
            "version_created": "2018-12-16T17:27:45.849208Z",
            "relevant_disorders": [
                "Familial non-syndromic cleft lip and or familial cleft palate",
                "Familial non-syndromic clefting",
                "Syndromic cleft lip and or cleft palate",
                "Syndromic clefting"
            ],
            "stats": {
                "number_of_regions": 5,
                "number_of_strs": 0,
                "number_of_genes": 252
            },
            "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."
                }
            ]
        },
        {
            "id": 64,
            "hash_id": "58ee38f88f62033bda307d54",
            "name": "ClinGen Gene Validity Curations",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.63",
            "version_created": "2017-11-05T02:37:19.953143Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 47
            },
            "types": [
                {
                    "name": "ClinGen Curated genes",
                    "slug": "clingen-curated-genes",
                    "description": "ClinGen Curated genes"
                }
            ]
        },
        {
            "id": 210,
            "hash_id": "594be3878f62037ee3e7e72f",
            "name": "ClinGen_Familial thoracic aortic aneurysm and aortic dissection",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.10",
            "version_created": "2017-11-05T02:37:20.232365Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 53
            },
            "types": [
                {
                    "name": "ClinGen Curated genes",
                    "slug": "clingen-curated-genes",
                    "description": "ClinGen Curated genes"
                }
            ]
        },
        {
            "id": 244,
            "hash_id": "596f84848f620352d0e3eeba",
            "name": "Colorectal cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.290684Z",
            "relevant_disorders": [
                "Colorectal"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 13
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 517,
            "hash_id": null,
            "name": "Combined factor V and VIII deficiency",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.19",
            "version_created": "2019-02-18T11:10:27.704337Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 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)"
                }
            ]
        },
        {
            "id": 507,
            "hash_id": null,
            "name": "Common craniosynostosis syndromes",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.1",
            "version_created": "2018-12-17T11:46:59.291175Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 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)"
                }
            ]
        },
        {
            "id": 508,
            "hash_id": null,
            "name": "Confirmed Fanconi anaemia or Bloom syndrome",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.20",
            "version_created": "2019-02-18T14:40:14.417471Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 22
            },
            "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)"
                }
            ]
        },
        {
            "id": 145,
            "hash_id": "55bf785822c1fc0fe45530bf",
            "name": "Congenital adrenal hypoplasia",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Adrenal disorders",
            "status": "public",
            "version": "1.7",
            "version_created": "2018-12-16T16:58:18.776512Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 20
            },
            "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."
                }
            ]
        },
        {
            "id": 25,
            "hash_id": "58346b8b8f62036225ca8a7d",
            "name": "Congenital disorders of glycosylation",
            "disease_group": "Metabolic disorders",
            "disease_sub_group": "Specific metabolic abnormalities",
            "status": "public",
            "version": "1.24",
            "version_created": "2019-02-18T15:21:48.987946Z",
            "relevant_disorders": [
                "Congential disorders of glycosylation"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 100
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 512,
            "hash_id": null,
            "name": "Congenital fibrosis of the extraocular muscles",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.6",
            "version_created": "2019-02-16T01:58:33.335174Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 5
            },
            "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)"
                }
            ]
        },
        {
            "id": 308,
            "hash_id": "553f9781bb5a1616e5ed45f4",
            "name": "Congenital hyperinsulinism",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Disorders of unusual phenotypes",
            "status": "public",
            "version": "1.39",
            "version_created": "2019-02-15T11:04:19.694295Z",
            "relevant_disorders": [
                "Hyperinsulinism"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 19
            },
            "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."
                }
            ]
        },
        {
            "id": 31,
            "hash_id": "5763f2938f620350a1996046",
            "name": "Congenital hypothyroidism",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Thyroid disorders",
            "status": "public",
            "version": "1.18",
            "version_created": "2019-01-17T15:06:32.839594Z",
            "relevant_disorders": [
                "Congenital hypothyroidism or thyroid agenesis"
            ],
            "stats": {
                "number_of_regions": 2,
                "number_of_strs": 0,
                "number_of_genes": 31
            },
            "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."
                }
            ]
        },
        {
            "id": 207,
            "hash_id": "55b117c022c1fc7dd7ce411c",
            "name": "Congenital muscular dystrophy",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neuromuscular disorders",
            "status": "public",
            "version": "1.21",
            "version_created": "2018-12-18T17:03:17.017138Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 1,
                "number_of_genes": 47
            },
            "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)"
                }
            ]
        },
        {
            "id": 232,
            "hash_id": "553f94c2bb5a1616e5ed459c",
            "name": "Congenital myaesthenic syndrome",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neuromuscular disorders",
            "status": "public",
            "version": "1.11",
            "version_created": "2018-12-17T11:00:28.896631Z",
            "relevant_disorders": [
                "Congenital myaesthenia",
                "Congenital myasthenia"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 29
            },
            "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)"
                }
            ]
        },
        {
            "id": 225,
            "hash_id": "553f94b6bb5a1616e5ed459a",
            "name": "Congenital myopathy",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neuromuscular disorders",
            "status": "public",
            "version": "1.72",
            "version_created": "2019-01-08T18:20:34.823598Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 3,
                "number_of_strs": 2,
                "number_of_genes": 92
            },
            "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)"
                }
            ]
        },
        {
            "id": 250,
            "hash_id": "553f979ebb5a1616e5ed45f6",
            "name": "Corneal dystrophy",
            "disease_group": "Ophthalmological disorders",
            "disease_sub_group": "Anterior segment abnormalities",
            "status": "public",
            "version": "1.6",
            "version_created": "2018-12-16T18:22:29.047386Z",
            "relevant_disorders": [
                "Corneal abnormalities"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 42
            },
            "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)"
                }
            ]
        },
        {
            "id": 168,
            "hash_id": "55b605f722c1fc05fd2345af",
            "name": "Craniosynostosis",
            "disease_group": "Skeletal disorders",
            "disease_sub_group": "Craniosynostosis syndromes",
            "status": "public",
            "version": "1.48",
            "version_created": "2019-03-07T10:32:08.919675Z",
            "relevant_disorders": [
                "Craniosynostosis syndromes",
                "Craniosynostosis syndromes phenotypes",
                "Rare syndromic craniosynostosis or isolated multisuture synostosis"
            ],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 110
            },
            "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."
                }
            ]
        },
        {
            "id": 5,
            "hash_id": "5763f3788f620350a199604a",
            "name": "Currarino triad",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.1",
            "version_created": "2017-11-05T02:37:19.823394Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 11
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 560,
            "hash_id": null,
            "name": "Cutaneous photosensitivity with a likely genetic cause",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.2",
            "version_created": "2018-12-20T15:08:48.391550Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 283,
            "hash_id": "55a646ef22c1fc6710839b9a",
            "name": "Cystic kidney disease",
            "disease_group": "Renal and urinary tract disorders",
            "disease_sub_group": "Structural renal and urinary tract disease",
            "status": "public",
            "version": "1.36",
            "version_created": "2019-01-30T14:18:22.196803Z",
            "relevant_disorders": [
                "Cystic kidney disease"
            ],
            "stats": {
                "number_of_regions": 2,
                "number_of_strs": 0,
                "number_of_genes": 60
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 487,
            "hash_id": null,
            "name": "Cystic renal disease",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.7",
            "version_created": "2019-02-01T14:32:26.894271Z",
            "relevant_disorders": [
                "Cystic renal disease - PKD1"
            ],
            "stats": {
                "number_of_regions": 4,
                "number_of_strs": 0,
                "number_of_genes": 260
            },
            "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"
                }
            ]
        },
        {
            "id": 159,
            "hash_id": "58a70e858f62037e8779b2e8",
            "name": "Cytopaenias and congenital anaemias",
            "disease_group": "Haematological disorders",
            "disease_sub_group": "Anaemias and red cell disorders",
            "status": "public",
            "version": "1.67",
            "version_created": "2019-03-06T14:17:24.081643Z",
            "relevant_disorders": [
                "Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuria",
                "Apparent aplastic anaemia or paroxysmal nocturnal haemoglobinuria",
                "Congenital anaemias",
                "Early onset pancytopenia and red cell disorders",
                "Anaemias and red cell disorders"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 217
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 520,
            "hash_id": null,
            "name": "Cytopenia - Fanconi breakage testing indicated",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.1",
            "version_created": "2018-12-17T13:28:06.291601Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 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)"
                }
            ]
        },
        {
            "id": 519,
            "hash_id": null,
            "name": "Cytopenia - NOT Fanconi anaemia",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.31",
            "version_created": "2019-02-18T14:57:00.051333Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 84
            },
            "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)"
                }
            ]
        },
        {
            "id": 484,
            "hash_id": null,
            "name": "DDG2P",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.8",
            "version_created": "2019-03-18T09:59:42.641410Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 1793
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 251,
            "hash_id": "57f4dbd18f62036d37cfe4e4",
            "name": "Deafness and congenital structural abnormalities",
            "disease_group": "Hearing and ear disorders",
            "disease_sub_group": "Deafness and congenital structural abnormalities",
            "status": "public",
            "version": "1.16",
            "version_created": "2019-01-28T09:59:52.697275Z",
            "relevant_disorders": [
                "Bilateral microtia",
                "Ear malformations with hearing impairment",
                "Ear malformations",
                "Familial hemifacial microsomia"
            ],
            "stats": {
                "number_of_regions": 3,
                "number_of_strs": 0,
                "number_of_genes": 54
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 293,
            "hash_id": "55a9041e22c1fc6711b0c6c0",
            "name": "Diabetes - neonatal onset",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Disorders of unusual phenotypes",
            "status": "public",
            "version": "1.24",
            "version_created": "2019-01-28T10:24:13.872434Z",
            "relevant_disorders": [
                "Neonatal diabetes (diagnosed less than 6 months)",
                "Neonatal diabetes",
                "Neonatal diabetes diagnosed <6 months"
            ],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 33
            },
            "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."
                }
            ]
        },
        {
            "id": 26,
            "hash_id": "55a9238422c1fc6711b0c6c3",
            "name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Disorders of unusual phenotypes",
            "status": "public",
            "version": "1.57",
            "version_created": "2018-12-20T17:47:53.259548Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 64
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 47,
            "hash_id": "55a4d99022c1fc6710839b84",
            "name": "Dilated cardiomyopathy - teen and adult",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Cardiomyopathy",
            "status": "public",
            "version": "1.49",
            "version_created": "2019-03-08T16:43:05.299401Z",
            "relevant_disorders": [
                "Dilated Cardiomyopathy and conduction defects",
                "Dilated Cardiomyopathy",
                "Dilated Cardiomyopathy (DCM)"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 84
            },
            "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)"
                }
            ]
        },
        {
            "id": 9,
            "hash_id": "569380ac22c1fc251660faf8",
            "name": "Disorders of sex development",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Gonadal and sex development disorders",
            "status": "public",
            "version": "1.31",
            "version_created": "2019-01-17T14:14:15.413888Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 53
            },
            "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."
                }
            ]
        },
        {
            "id": 235,
            "hash_id": "55b7a0bb22c1fc05fd2345d1",
            "name": "Distal myopathies",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neuromuscular disorders",
            "status": "public",
            "version": "1.10",
            "version_created": "2018-12-07T10:42:59.172248Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 2,
                "number_of_genes": 27
            },
            "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."
                }
            ]
        },
        {
            "id": 209,
            "hash_id": "58c8066b8f6203413360f1cf",
            "name": "Ductal plate malformation",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.9",
            "version_created": "2019-03-12T11:20:30.057909Z",
            "relevant_disorders": [
                "Ductal plate malformation (DPM)",
                "Polycystic liver disease"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 150
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 475,
            "hash_id": null,
            "name": "Dystonia - childhood onset",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.2",
            "version_created": "2019-02-12T12:33:55.218922Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 7,
                "number_of_genes": 176
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 265,
            "hash_id": "55b6173522c1fc05fc7a1855",
            "name": "Early onset dementia (encompassing fronto-temporal dementia and prion disease)",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neurodegenerative disorders",
            "status": "public",
            "version": "1.46",
            "version_created": "2018-12-20T17:00:18.301209Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 9,
                "number_of_genes": 31
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 192,
            "hash_id": "553f95c9bb5a1616e5ed45bf",
            "name": "Early onset dystonia",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Motor Disorders of the CNS",
            "status": "public",
            "version": "1.78",
            "version_created": "2019-01-09T14:29:33.686208Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 4,
                "number_of_genes": 110
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 553,
            "hash_id": null,
            "name": "Ectodermal dysplasia",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.10",
            "version_created": "2019-01-31T16:06:22.355977Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 61
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 136,
            "hash_id": "561677af22c1fc212a6db65d",
            "name": "Ectodermal dysplasia without a known gene mutation",
            "disease_group": "Dermatological disorders",
            "disease_sub_group": "Ectodermal dysplasias",
            "status": "public",
            "version": "1.17",
            "version_created": "2019-01-31T16:11:38.565404Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 29
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 53,
            "hash_id": "588728f38f62030cf7152165",
            "name": "Ehlers Danlos syndromes",
            "disease_group": "Rheumatological disorders",
            "disease_sub_group": "Connective tissues disorders",
            "status": "public",
            "version": "1.41",
            "version_created": "2019-03-13T11:26:58.887194Z",
            "relevant_disorders": [
                "Classical Ehlers Danlos Syndrome",
                "Ehlers-Danlos Syndrome (unusual phenotypes e.g. absent pain sense)",
                "Ehlers-Danlos syndrome type 3",
                "Kyphoscoliotic Ehlers-Danlos syndrome",
                "EDS",
                "Ehlers-Danlos syndromes"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 75
            },
            "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."
                }
            ]
        },
        {
            "id": 156,
            "hash_id": "5693974122c1fc251660fb1f",
            "name": "End-stage renal disease - childhood onset",
            "disease_group": "Renal and urinary tract disorders",
            "disease_sub_group": "Disorders of function",
            "status": "public",
            "version": "1.62",
            "version_created": "2019-01-30T15:25:49.564022Z",
            "relevant_disorders": [
                "Unexplained kidney failure in young people",
                "Familial IgA nephropathy and IgA vasculitis"
            ],
            "stats": {
                "number_of_regions": 3,
                "number_of_strs": 0,
                "number_of_genes": 166
            },
            "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."
                }
            ]
        },
        {
            "id": 648,
            "hash_id": null,
            "name": "Endocrine neoplasms",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.4",
            "version_created": "2019-03-11T14:02:30.944946Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 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."
                }
            ]
        },
        {
            "id": 271,
            "hash_id": "596f859c8f620352d0e3eec9",
            "name": "Endometrial cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.335660Z",
            "relevant_disorders": [
                "Endometrial Carcinoma"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 6
            },
            "types": [
                {
                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
            "id": 562,
            "hash_id": null,
            "name": "Epidermodysplasia verruciformis",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.5",
            "version_created": "2019-02-18T14:25:20.217430Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 3
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 119,
            "hash_id": "56310b9a22c1fc58285b282c",
            "name": "Epidermolysis bullosa",
            "disease_group": "Dermatological disorders",
            "disease_sub_group": "Skin fragility disorders",
            "status": "public",
            "version": "1.6",
            "version_created": "2019-01-07T16:40:38.182703Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 21
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 554,
            "hash_id": null,
            "name": "Epidermolysis bullosa and congenital skin fragility",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "0.11",
            "version_created": "2019-01-10T09:38:43.112563Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 34
            },
            "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": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                }
            ]
        },
        {
            "id": 489,
            "hash_id": null,
            "name": "Epilepsy - early onset or syndromic",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "2.78",
            "version_created": "2019-03-18T12:16:36.513383Z",
            "relevant_disorders": [
                "Early onset or syndromic epilepsy"
            ],
            "stats": {
                "number_of_regions": 14,
                "number_of_strs": 4,
                "number_of_genes": 1439
            },
            "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"
                }
            ]
        },
        {
            "id": 91,
            "hash_id": "553f9599bb5a1616e5ed45af",
            "name": "Erythropoietic protoporphyria, mild variant",
            "disease_group": "Dermatological disorders",
            "disease_sub_group": "Sun-exposure related conditions",
            "status": "public",
            "version": "1.2",
            "version_created": "2017-11-05T02:37:20.011517Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 2
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 314,
            "hash_id": "553f9697bb5a1616e5ed45d4",
            "name": "Extreme early-onset hypertension",
            "disease_group": "Renal and urinary tract disorders",
            "disease_sub_group": "Disorders of function",
            "status": "public",
            "version": "1.10",
            "version_created": "2018-12-16T17:33:34.572280Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 25
            },
            "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."
                }
            ]
        },
        {
            "id": 63,
            "hash_id": "58c7f5008f620328d77ce70f",
            "name": "Familial Hirschsprung Disease",
            "disease_group": "Gastroenterological disorders",
            "disease_sub_group": "Gastrointestinal disorders",
            "status": "public",
            "version": "1.5",
            "version_created": "2017-11-05T02:37:19.951460Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 62
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 394,
            "hash_id": null,
            "name": "Familial Meniere Disease",
            "disease_group": "Hearing and ear disorders",
            "disease_sub_group": "Other hearing and ear disorders",
            "status": "public",
            "version": "1.1",
            "version_created": "2018-01-17T16:26:29.432517Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 130
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 11,
            "hash_id": "57e3df7e8f62034b82c0d332",
            "name": "Familial Neural Tube Defects",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.5",
            "version_created": "2017-11-05T02:37:19.836037Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 44
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 167,
            "hash_id": "55af764522c1fc78a829f89a",
            "name": "Familial Tumours Syndromes of the central & peripheral Nervous system",
            "disease_group": "Tumour syndromes",
            "disease_sub_group": "Muscle and nerve",
            "status": "public",
            "version": "1.8",
            "version_created": "2017-11-05T02:37:20.155455Z",
            "relevant_disorders": [
                "Familial tumour syndromes of the central & peripheral nervous system",
                "Familial tumour syndromes of the central and peripheral nervous system"
            ],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 21
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 158,
            "hash_id": "55b62bc422c1fc05fc7a1857",
            "name": "Familial breast cancer",
            "disease_group": "Tumour syndromes",
            "disease_sub_group": "Breast and endocrine",
            "status": "public",
            "version": "1.13",
            "version_created": "2017-11-05T02:37:20.139339Z",
            "relevant_disorders": [
                "Familial breast and or ovarian cancer"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 26
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 50,
            "hash_id": "5693787622c1fc25158f3c9a",
            "name": "Familial cerebral small vessel disease",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Arteriopathies",
            "status": "public",
            "version": "1.6",
            "version_created": "2019-01-20T15:15:42.512731Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 16
            },
            "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."
                }
            ]
        },
        {
            "id": 305,
            "hash_id": "568e844522c1fc1c78b67156",
            "name": "Familial cicatricial alopecia",
            "disease_group": "Dermatological disorders",
            "disease_sub_group": "Skin adnexa disorders",
            "status": "public",
            "version": "1.1",
            "version_created": "2017-11-05T02:37:20.395462Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 25
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 152,
            "hash_id": "553f9745bb5a1616e5ed45e9",
            "name": "Familial diabetes",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Disorders of unusual phenotypes",
            "status": "public",
            "version": "1.36",
            "version_created": "2019-03-01T14:23:14.159020Z",
            "relevant_disorders": [
                "Familial young-onset non-insulin-dependent diabetes"
            ],
            "stats": {
                "number_of_regions": 1,
                "number_of_strs": 0,
                "number_of_genes": 56
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 110,
            "hash_id": "5763f6048f620350a1996052",
            "name": "Familial disseminated superficial actinic porokeratosis",
            "disease_group": "Dermatological disorders",
            "disease_sub_group": "Keratodermas",
            "status": "public",
            "version": "1.1",
            "version_created": "2017-11-05T02:37:20.048842Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 7
            },
            "types": [
                {
                    "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": "1.5",
            "version_created": "2018-11-16T08:54:22.201084Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 22
            },
            "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."
                }
            ]
        },
        {
            "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_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 11
            },
            "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": "1.21",
            "version_created": "2018-12-16T16:24:40.515333Z",
            "relevant_disorders": [
                "Familial Hypercholesterolaemia",
                "Familial Hypercholesterolemia"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 43
            },
            "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."
                }
            ]
        },
        {
            "id": 480,
            "hash_id": null,
            "name": "Familial hyperparathyroidism",
            "disease_group": "",
            "disease_sub_group": "",
            "status": "public",
            "version": "1.0",
            "version_created": "2019-01-30T11:28:51.074300Z",
            "relevant_disorders": [],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 10
            },
            "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."
                }
            ]
        },
        {
            "id": 312,
            "hash_id": "55bf826222c1fc0fe45530c1",
            "name": "Familial hypoparathyroidism",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Disorders of calcium homeostasis",
            "status": "public",
            "version": "1.10",
            "version_created": "2019-01-10T14:37:33.031659Z",
            "relevant_disorders": [
                "Familial or syndromic hypoparathyroidism"
            ],
            "stats": {
                "number_of_regions": 0,
                "number_of_strs": 0,
                "number_of_genes": 9
            },
            "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."
                }
            ]
        }
    ]
}