GET /WebServices/list_panels/
HTTP 200 OK
Allow: GET, OPTIONS
Content-Type: application/json
Vary: Accept

{
    "result": [
        {
            "Panel_Id": "5596735822c1fc4f7d26e96d",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
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            "Number_of_Genes": 58,
            "Name": "Thoracic aortic aneurysm or dissection",
            "Status": "public",
            "CurrentCreated": "2018-12-16T16:23:12.982701Z",
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                "Familial retinal arteriolar tortuosity",
                "FTAAD",
                "Familial Thoracic Aortic Aneurysm Disease"
            ]
        },
        {
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            "CurrentCreated": "2018-12-16T18:24:14.098733Z",
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            "CurrentCreated": "2018-12-16T16:24:40.515333Z",
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        },
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            "CurrentCreated": "2018-11-19T13:23:59.404588Z",
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            "Name": "Chondrodysplasia punctata",
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            "CurrentCreated": "2017-11-05T02:37:19.878296Z",
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            "CurrentCreated": "2018-12-19T13:30:04.102060Z",
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            "Name": "Gastrointestinal epithelial barrier disorders",
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            "Name": "Anophthalmia or microphthalmia",
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            "CurrentCreated": "2018-11-05T09:04:34.272011Z",
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            "Name": "Endocrine neoplasia",
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            "CurrentCreated": "2018-12-16T17:10:16.833416Z",
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            "Name": "Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders",
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            "Name": "Parkinson Disease and Complex Parkinsonism",
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            "Name": "Inherited white matter disorders",
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            "CurrentCreated": "2018-12-19T13:57:29.480979Z",
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            "Name": "Sudden death in young people",
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            "CurrentCreated": "2018-11-01T15:21:31.296785Z",
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            "Name": "Dilated cardiomyopathy - teen and adult",
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            "CurrentCreated": "2018-12-16T18:19:12.251698Z",
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            "Name": "RASopathies",
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            "CurrentCreated": "2017-11-05T02:37:19.917137Z",
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            "DiseaseGroup": "Dysmorphic and congenital abnormality syndromes",
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            "Relevant_disorders": [
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                "Costello syndrome",
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            "Name": "Hypertrophic cardiomyopathy - teen and adult",
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            "CurrentCreated": "2018-12-16T18:16:58.626638Z",
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            "Name": "Familial cerebral small vessel disease",
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            "CurrentCreated": "2018-12-16T17:40:36.453812Z",
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            "DiseaseGroup": "Cardiovascular disorders",
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            "Number_of_Genes": 75,
            "Name": "Ehlers Danlos syndromes",
            "Status": "public",
            "CurrentCreated": "2018-12-14T16:06:12.553685Z",
            "CurrentVersion": "1.39",
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                "Ehlers-Danlos Syndrome (unusual phenotypes e.g. absent pain sense)",
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                "Ehlers-Danlos syndromes"
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            "Number_of_Genes": 30,
            "Name": "Periodic fever syndromes",
            "Status": "public",
            "CurrentCreated": "2017-11-05T02:37:19.944602Z",
            "CurrentVersion": "1.10",
            "DiseaseGroup": "Rheumatological disorders",
            "DiseaseSubGroup": "Multi-system inflammatory/autoimmune disorders",
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            "Number_of_Genes": 26,
            "Name": "Gastrointestinal neuromuscular disorders",
            "Status": "public",
            "CurrentCreated": "2018-12-16T17:39:16.981966Z",
            "CurrentVersion": "1.10",
            "DiseaseGroup": "Gastroenterological disorders",
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            "Relevant_disorders": [
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            "Number_of_Genes": 8,
            "Name": "Severe multi-system atopic disease with high IgE",
            "Status": "public",
            "CurrentCreated": "2017-11-05T02:37:19.949470Z",
            "CurrentVersion": "1.7",
            "DiseaseGroup": "Dermatological disorders",
            "DiseaseSubGroup": "Atopy",
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            "Number_of_Genes": 62,
            "Name": "Familial Hirschsprung Disease",
            "Status": "public",
            "CurrentCreated": "2017-11-05T02:37:19.951460Z",
            "CurrentVersion": "1.5",
            "DiseaseGroup": "Gastroenterological disorders",
            "DiseaseSubGroup": "Gastrointestinal disorders",
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        {
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            "Number_of_Genes": 22,
            "Name": "Primary lymphoedema",
            "Status": "public",
            "CurrentCreated": "2018-12-16T16:27:37.437745Z",
            "CurrentVersion": "1.33",
            "DiseaseGroup": "Cardiovascular disorders",
            "DiseaseSubGroup": "Lymphatic Disorders",
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Relevant_disorders": [
                "Lymphatic Disorders",
                "Meiges disease",
                "Meige disease",
                "Milroy disease",
                "Lymphoedema distichiasis",
                "Lipoedema disease"
            ]
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        {
            "Panel_Id": "55b63d7f22c1fc05fc7a185b",
            "PanelTypes": [
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            "Number_of_Genes": 55,
            "Name": "Rhabdomyolysis and metabolic muscle disorders",
            "Status": "public",
            "CurrentCreated": "2018-12-16T17:31:04.931886Z",
            "CurrentVersion": "1.23",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Relevant_disorders": []
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        {
            "Panel_Id": "55bf939f22c1fc0fe45530c4",
            "PanelTypes": [
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            "Number_of_Genes": 18,
            "Name": "Mucopolysaccharideosis, Gaucher, Fabry",
            "Status": "public",
            "CurrentCreated": "2017-11-05T02:37:19.973980Z",
            "CurrentVersion": "1.2",
            "DiseaseGroup": "Metabolic disorders",
            "DiseaseSubGroup": "Lysosomal storage disorders",
            "Number_of_STRs": 0,
            "Number_of_Regions": null,
            "Relevant_disorders": []
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        {
            "Panel_Id": "55a3b19722c1fc6710839b80",
            "PanelTypes": [
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                "rare-disease-100k"
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            "Number_of_Genes": 20,
            "Name": "Long QT syndrome",
            "Status": "public",
            "CurrentCreated": "2018-12-16T18:07:20.930919Z",
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