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

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            "hash_id": "55a39e2d22c1fc6711b0c6b3",
            "name": "Hypertrophic cardiomyopathy - teen and adult",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Cardiomyopathy",
            "status": "public",
            "version": "1.26",
            "version_created": "2018-12-16T18:16:58.626638Z",
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                "HCM"
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                "number_of_regions": 0,
                "number_of_strs": 1
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                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease",
                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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        },
        {
            "id": 50,
            "hash_id": "5693787622c1fc25158f3c9a",
            "name": "Familial cerebral small vessel disease",
            "disease_group": "Cardiovascular disorders",
            "disease_sub_group": "Arteriopathies",
            "status": "public",
            "version": "1.5",
            "version_created": "2018-12-16T17:40:36.453812Z",
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            "stats": {
                "number_of_genes": 15,
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                "number_of_strs": 0
            },
            "types": [
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                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
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        },
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            "name": "Ehlers Danlos syndromes",
            "disease_group": "Rheumatological disorders",
            "disease_sub_group": "Connective tissues disorders",
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            "version": "1.40",
            "version_created": "2019-01-08T18:19:45.177611Z",
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                "Ehlers-Danlos Syndrome (unusual phenotypes e.g. absent pain sense)",
                "Ehlers-Danlos syndrome type 3",
                "Kyphoscoliotic Ehlers-Danlos syndrome",
                "EDS",
                "Ehlers-Danlos syndromes"
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            "stats": {
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                "number_of_strs": 0
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                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                }
            ]
        },
        {
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            "disease_group": "Cancer Programme",
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            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:19.933392Z",
            "relevant_disorders": [
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            },
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                    "name": "Cancer Germline 100K",
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                    "description": "Cancer Germline 100K"
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            "name": "Haematological malignancies pertinent cancer susceptibility",
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            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.2",
            "version_created": "2017-11-05T02:37:19.942373Z",
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            ],
            "stats": {
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                "number_of_regions": 0,
                "number_of_strs": 0
            },
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                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
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            "name": "Periodic fever syndromes",
            "disease_group": "Rheumatological disorders",
            "disease_sub_group": "Multi-system inflammatory/autoimmune disorders",
            "status": "public",
            "version": "1.10",
            "version_created": "2017-11-05T02:37:19.944602Z",
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            "version_created": "2018-12-16T17:39:16.981966Z",
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                "number_of_strs": 1
            },
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                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                }
            ]
        },
        {
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            "name": "Severe multi-system atopic disease with high IgE",
            "disease_group": "Dermatological disorders",
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            "status": "public",
            "version": "1.7",
            "version_created": "2017-11-05T02:37:19.949470Z",
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            "version": "1.5",
            "version_created": "2017-11-05T02:37:19.951460Z",
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            "version": "0.63",
            "version_created": "2017-11-05T02:37:19.953143Z",
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            },
            "types": [
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                    "name": "ClinGen Curated genes",
                    "slug": "clingen-curated-genes",
                    "description": "ClinGen Curated genes"
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            "version": "1.33",
            "version_created": "2018-12-16T16:27:37.437745Z",
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                "Meige disease",
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                "Lipoedema disease"
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            },
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                },
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                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                }
            ]
        },
        {
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            "name": "Rhabdomyolysis and metabolic muscle disorders",
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            "version": "1.25",
            "version_created": "2019-01-08T18:21:44.771539Z",
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                },
                {
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                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                }
            ]
        },
        {
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            "name": "Mucopolysaccharideosis, Gaucher, Fabry",
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            "version": "1.2",
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            ]
        },
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        },
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            ]
        },
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            ]
        },
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        },
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            "version": "1.20",
            "version_created": "2019-01-16T13:48:18.989732Z",
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
                }
            ]
        },
        {
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            "name": "Fetal hydrops",
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            "disease_sub_group": "Fetal disorders",
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            "version": "1.16",
            "version_created": "2018-12-05T18:38:09.145885Z",
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                "number_of_strs": 1
            },
            "types": [
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                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
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            ]
        },
        {
            "id": 145,
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            "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",
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            "stats": {
                "number_of_genes": 20,
                "number_of_regions": 0,
                "number_of_strs": 0
            },
            "types": [
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                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                }
            ]
        },
        {
            "id": 147,
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            "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": [
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                "Vein of Galen malformation",
                "Cerebral arteriovenous malformations",
                "Moyamoya disease"
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                "number_of_regions": 0,
                "number_of_strs": 0
            },
            "types": [
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                    "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."
                }
            ]
        },
        {
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            "version": "1.16",
            "version_created": "2018-12-17T10:48:57.615031Z",
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                "number_of_regions": 0,
                "number_of_strs": 0
            },
            "types": [
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                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease",
                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            ]
        },
        {
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            "name": "Rare multisystem ciliopathy disorders",
            "disease_group": "Ciliopathies",
            "disease_sub_group": "Congenital malformations caused by ciliopathies",
            "status": "public",
            "version": "1.83",
            "version_created": "2018-12-20T14:12:18.444102Z",
            "relevant_disorders": [
                "Joubert syndrome",
                "Bardet-Biedl Syndrome"
            ],
            "stats": {
                "number_of_genes": 200,
                "number_of_regions": 2,
                "number_of_strs": 0
            },
            "types": [
                {
                    "name": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
                },
                {
                    "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."
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            ]
        },
        {
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            "name": "Familial diabetes",
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            "status": "public",
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            "version_created": "2018-12-20T17:48:20.765163Z",
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                "Familial young-onset non-insulin-dependent diabetes"
            ],
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                "number_of_regions": 1,
                "number_of_strs": 0
            },
            "types": [
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                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
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            ]
        },
        {
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            "name": "Renal cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.131112Z",
            "relevant_disorders": [
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            ],
            "stats": {
                "number_of_genes": 10,
                "number_of_strs": 0
            },
            "types": [
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                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
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            "name": "Primary ovarian insufficiency",
            "disease_group": "Endocrine disorders",
            "disease_sub_group": "Gonadal and sex development disorders",
            "status": "public",
            "version": "1.15",
            "version_created": "2018-12-16T17:32:16.357555Z",
            "relevant_disorders": [
                "Early onset familial premature ovarian insufficiency",
                "Early onset familial premature ovarian failure"
            ],
            "stats": {
                "number_of_genes": 56,
                "number_of_regions": 0,
                "number_of_strs": 1
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                }
            ]
        },
        {
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            "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": "1.23",
            "version_created": "2018-12-16T17:23:14.766026Z",
            "relevant_disorders": [
                "Unexplained kidney failure in young people",
                "Familial IgA nephropathy and IgA vasculitis"
            ],
            "stats": {
                "number_of_genes": 166,
                "number_of_regions": 3,
                "number_of_strs": 0
            },
            "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."
                }
            ]
        },
        {
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            "name": "Hereditary Erythrocytosis",
            "disease_group": "",
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            "status": "public",
            "version": "1.1",
            "version_created": "2017-11-05T02:37:20.137591Z",
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            "stats": {
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            },
            "types": [
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                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
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            ]
        },
        {
            "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",
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            },
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            ]
        },
        {
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            "name": "Cytopaenias and congenital anaemias",
            "disease_group": "Haematological disorders",
            "disease_sub_group": "Anaemias and red cell disorders",
            "status": "public",
            "version": "1.65",
            "version_created": "2017-11-05T02:37:20.141069Z",
            "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": {
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                "number_of_strs": 0
            },
            "types": [
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                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                }
            ]
        },
        {
            "id": 162,
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            "name": "Severe microcephaly",
            "disease_group": "Dysmorphic and congenital abnormality syndromes",
            "disease_sub_group": "DNA repair disorders",
            "status": "public",
            "version": "1.44",
            "version_created": "2018-12-17T16:02:44.176340Z",
            "relevant_disorders": [
                "Primary Microcephaly - Microcephalic Dwarfism Spectrum",
                "Severe microcephaly"
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                "number_of_regions": 4,
                "number_of_strs": 0
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            "types": [
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                    "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."
                }
            ]
        },
        {
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            "disease_sub_group": "Motor Disorders of the CNS",
            "status": "public",
            "version": "1.185",
            "version_created": "2019-01-14T09:43:24.132278Z",
            "relevant_disorders": [],
            "stats": {
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                "number_of_regions": 0,
                "number_of_strs": 10
            },
            "types": [
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                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
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            ]
        },
        {
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            "name": "Brain cancer pertinent cancer susceptibility",
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            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
            "status": "public",
            "version": "1.0",
            "version_created": "2017-11-05T02:37:20.153599Z",
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            "stats": {
                "number_of_genes": 7,
                "number_of_strs": 0
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            "types": [
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                    "name": "Cancer Germline 100K",
                    "slug": "cancer-germline-100k",
                    "description": "Cancer Germline 100K"
                }
            ]
        },
        {
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            "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": [
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                "Familial tumour syndromes of the central and peripheral nervous system"
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            "stats": {
                "number_of_genes": 21,
                "number_of_regions": 1,
                "number_of_strs": 0
            },
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        },
        {
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            "name": "Craniosynostosis",
            "disease_group": "Skeletal disorders",
            "disease_sub_group": "Craniosynostosis syndromes",
            "status": "public",
            "version": "1.44",
            "version_created": "2018-12-17T15:47:11.316091Z",
            "relevant_disorders": [
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                "Craniosynostosis syndromes phenotypes",
                "Rare syndromic craniosynostosis or isolated multisuture synostosis"
            ],
            "stats": {
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                "number_of_regions": 1,
                "number_of_strs": 0
            },
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                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                }
            ]
        },
        {
            "id": 171,
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            "name": "Inherited non-medullary thyroid cancer",
            "disease_group": "Tumour syndromes",
            "disease_sub_group": "Breast and endocrine",
            "status": "public",
            "version": "1.4",
            "version_created": "2017-11-05T02:37:20.162547Z",
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        },
        {
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            "name": "Kabuki syndrome",
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            "disease_sub_group": "Kabuki",
            "status": "public",
            "version": "1.2",
            "version_created": "2017-11-05T02:37:20.165958Z",
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        }
    ]
}