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

{
    "result": [
        {
            "DiseaseGroup": "Tumour syndromes",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.21",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Young adult onset cancer",
                "Exceptionally young adult onset cancer",
                "Multiple Tumours",
                "Rare tumour predisposition syndromes"
            ],
            "DiseaseSubGroup": "Tumour syndromes",
            "CurrentCreated": "2018-12-11T12:56:38.497201Z",
            "Panel_Id": "391",
            "Status": "public",
            "Number_of_Regions": 1,
            "Number_of_Genes": 58,
            "Name": "Adult solid tumours for rare disease"
        },
        {
            "DiseaseGroup": "Skeletal disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.7",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Amelogenesis Imperfecta"
            ],
            "DiseaseSubGroup": "Skeletal dysplasias",
            "CurrentCreated": "2018-12-17T09:55:36.360380Z",
            "Panel_Id": "58c7f3c78f620328d77ce70e",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 39,
            "Name": "Amelogenesis imperfecta"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.26",
            "Number_of_STRs": 4,
            "Relevant_disorders": [
                "Amyotrophic lateral sclerosis or motor neuron disease"
            ],
            "DiseaseSubGroup": "Neurodegenerative disorders",
            "CurrentCreated": "2018-12-07T11:43:08.799661Z",
            "Panel_Id": "55d30b0322c1fc2ff2a5bf7b",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 30,
            "Name": "Amyotrophic lateral sclerosis/motor neuron disease"
        },
        {
            "DiseaseGroup": "Ophthalmological disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.17",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Anophthalmia or microphthamia",
                "Anophthalmia/microphthamia",
                "Anophthalmia/microphthalmia"
            ],
            "DiseaseSubGroup": "Ocular malformations",
            "CurrentCreated": "2019-02-15T11:47:13.583658Z",
            "Panel_Id": "553f97abbb5a1616e5ed45f9",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 57,
            "Name": "Anophthalmia or microphthalmia"
        },
        {
            "DiseaseGroup": "Cardiovascular disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.17",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Arrhythmogenic Right Ventricular Cardiomyopathy",
                "Arrythmogenic cardiomyopathy"
            ],
            "DiseaseSubGroup": "Cardiomyopathy",
            "CurrentCreated": "2019-02-14T13:38:36.022177Z",
            "Panel_Id": "55a3876e22c1fc63fec6d0da",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 16,
            "Name": "Arrhythmogenic cardiomyopathy"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "2.37",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Arthrogrythsis"
            ],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2019-01-08T17:28:10.298059Z",
            "Panel_Id": "55b75d5b22c1fc05fd2345c9",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 245,
            "Name": "Arthrogryposis"
        },
        {
            "DiseaseGroup": "Renal and urinary tract disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.7",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Syndromes with prominent renal abnormalities",
            "CurrentCreated": "2019-02-12T12:40:42.563719Z",
            "Panel_Id": "563248da22c1fc58285b283a",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 13,
            "Name": "Atypical haemolytic uraemic syndrome"
        },
        {
            "DiseaseGroup": "Hearing and ear disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.5",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Auditory Neuropathy Spectrum Disorder",
                "Auditory Neuropathy Spectrum Disorde"
            ],
            "DiseaseSubGroup": "Non-syndromic hearing loss",
            "CurrentCreated": "2017-11-05T02:37:20.316932Z",
            "Panel_Id": "55b20bdf22c1fc7dd6b9bbb7",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 5,
            "Name": "Auditory Neuropathy Spectrum Disorder"
        },
        {
            "DiseaseGroup": "Dermatological disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.7",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Ichthyoses",
            "CurrentCreated": "2017-11-05T02:37:20.354821Z",
            "Panel_Id": "562e5d2622c1fc582756e3b5",
            "Status": "public",
            "Number_of_Regions": 1,
            "Number_of_Genes": 14,
            "Name": "Autosomal recessive congenital ichthyosis"
        },
        {
            "DiseaseGroup": "Growth disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.42",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Atypical Beckwith-Wiedemann syndrome",
                "Classical Beckwith-Wiedemann syndrome",
                "Simpson-Golabi-Behmel syndrome",
                "Sotos syndrome",
                "Weaver syndrome"
            ],
            "DiseaseSubGroup": "Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders",
            "CurrentCreated": "2017-11-05T02:37:19.894933Z",
            "Panel_Id": "56fa8eb88f62030f36e3026b",
            "Status": "public",
            "Number_of_Regions": 1,
            "Number_of_Genes": 19,
            "Name": "Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.52",
            "Number_of_STRs": 5,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Channelopathies",
            "CurrentCreated": "2019-01-09T13:43:39.338221Z",
            "Panel_Id": "55c2321822c1fc0fe5e416e1",
            "Status": "public",
            "Number_of_Regions": 1,
            "Number_of_Genes": 24,
            "Name": "Brain channelopathy"
        },
        {
            "DiseaseGroup": "Cardiovascular disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.19",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "CurrentCreated": "2019-02-14T13:38:26.719825Z",
            "Panel_Id": "55a3a78122c1fc6711b0c6b5",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 23,
            "Name": "Brugada syndrome"
        },
        {
            "DiseaseGroup": "Renal and urinary tract disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.34",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Congenital Anomaly of the Kidneys and Urinary Tract (CAKUT)"
            ],
            "DiseaseSubGroup": "Structural renal and urinary tract disease",
            "CurrentCreated": "2019-01-30T15:05:14.897132Z",
            "Panel_Id": "553f9696bb5a1616e5ed45d1",
            "Status": "public",
            "Number_of_Regions": 1,
            "Number_of_Genes": 65,
            "Name": "CAKUT"
        },
        {
            "DiseaseGroup": "Ophthalmological disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.25",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "CurrentCreated": "2019-01-30T14:20:35.545988Z",
            "Panel_Id": "553f979fbb5a1616e5ed45f8",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 157,
            "Name": "Cataracts"
        },
        {
            "DiseaseGroup": "Cardiovascular disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.6",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Catecholaminergic Polymorphic Ventricular Tachycardia"
            ],
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "CurrentCreated": "2019-02-14T13:38:36.264481Z",
            "Panel_Id": "55a3aac122c1fc6710839b7d",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 9,
            "Name": "Catecholaminergic polymorphic VT"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.25",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Cerebellar Hypoplasia",
                "Pontine tegmental cap dysplasia"
            ],
            "DiseaseSubGroup": "Motor Disorders of the CNS",
            "CurrentCreated": "2018-12-03T11:25:19.110335Z",
            "Panel_Id": "568f871422c1fc1c79ca176d",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 64,
            "Name": "Cerebellar hypoplasia"
        },
        {
            "DiseaseGroup": "Metabolic disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.2",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Specific metabolic abnormalities",
            "CurrentCreated": "2017-11-05T02:37:20.047324Z",
            "Panel_Id": "55537918bb5a161bf644a3c7",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 4,
            "Name": "Cerebral folate deficiency"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.36",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Cerebrovascular disorders",
                "Vein of Galen malformation",
                "Cerebral arteriovenous malformations",
                "Moyamoya disease"
            ],
            "DiseaseSubGroup": "Cerebrovascular disorders",
            "CurrentCreated": "2018-12-16T17:21:50.776136Z",
            "Panel_Id": "5819a24f8f6203341de99c89",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 93,
            "Name": "Cerebral vascular malformations"
        },
        {
            "DiseaseGroup": "Skeletal disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.12",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Choanal anomalies",
            "CurrentCreated": "2017-11-05T02:37:20.252051Z",
            "Panel_Id": "553f9697bb5a1616e5ed45d3",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 12,
            "Name": "Choanal atresia"
        },
        {
            "DiseaseGroup": "Skeletal disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.2",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Skeletal dysplasias",
            "CurrentCreated": "2017-11-05T02:37:19.878296Z",
            "Panel_Id": "554a0ac9bb5a167e4ccd1ec0",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 5,
            "Name": "Chondrodysplasia punctata"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.2",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Neurodevelopmental disorders",
            "CurrentCreated": "2017-11-05T02:37:20.208587Z",
            "Panel_Id": "553f968cbb5a1616e5ed45cc",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 2,
            "Name": "Classical tuberous sclerosis"
        },
        {
            "DiseaseGroup": "Dysmorphic and congenital abnormality syndromes",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.34",
            "Number_of_STRs": 0,
            "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"
            ],
            "DiseaseSubGroup": "Dysmorphic disorders",
            "CurrentCreated": "2018-12-16T17:27:45.849208Z",
            "Panel_Id": "57acb8268f620364dc61afd3",
            "Status": "public",
            "Number_of_Regions": 5,
            "Number_of_Genes": 252,
            "Name": "Clefting"
        },
        {
            "DiseaseGroup": "Endocrine disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.7",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Adrenal disorders",
            "CurrentCreated": "2018-12-16T16:58:18.776512Z",
            "Panel_Id": "55bf785822c1fc0fe45530bf",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 20,
            "Name": "Congenital adrenal hypoplasia"
        },
        {
            "DiseaseGroup": "Metabolic disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.21",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Congential disorders of glycosylation"
            ],
            "DiseaseSubGroup": "Specific metabolic abnormalities",
            "CurrentCreated": "2019-01-24T16:46:28.679165Z",
            "Panel_Id": "58346b8b8f62036225ca8a7d",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 100,
            "Name": "Congenital disorders of glycosylation"
        },
        {
            "DiseaseGroup": "Endocrine disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.39",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Hyperinsulinism"
            ],
            "DiseaseSubGroup": "Disorders of unusual phenotypes",
            "CurrentCreated": "2019-02-15T11:04:19.694295Z",
            "Panel_Id": "553f9781bb5a1616e5ed45f4",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 19,
            "Name": "Congenital hyperinsulinism"
        },
        {
            "DiseaseGroup": "Endocrine disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.18",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Congenital hypothyroidism or thyroid agenesis"
            ],
            "DiseaseSubGroup": "Thyroid disorders",
            "CurrentCreated": "2019-01-17T15:06:32.839594Z",
            "Panel_Id": "5763f2938f620350a1996046",
            "Status": "public",
            "Number_of_Regions": 2,
            "Number_of_Genes": 31,
            "Name": "Congenital hypothyroidism"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.21",
            "Number_of_STRs": 1,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2018-12-18T17:03:17.017138Z",
            "Panel_Id": "55b117c022c1fc7dd7ce411c",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 47,
            "Name": "Congenital muscular dystrophy"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.11",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Congenital myaesthenia",
                "Congenital myasthenia"
            ],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2018-12-17T11:00:28.896631Z",
            "Panel_Id": "553f94c2bb5a1616e5ed459c",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 29,
            "Name": "Congenital myaesthenic syndrome"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.72",
            "Number_of_STRs": 2,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2019-01-08T18:20:34.823598Z",
            "Panel_Id": "553f94b6bb5a1616e5ed459a",
            "Status": "public",
            "Number_of_Regions": 3,
            "Number_of_Genes": 92,
            "Name": "Congenital myopathy"
        },
        {
            "DiseaseGroup": "Ophthalmological disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.6",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Corneal abnormalities"
            ],
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "CurrentCreated": "2018-12-16T18:22:29.047386Z",
            "Panel_Id": "553f979ebb5a1616e5ed45f6",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 42,
            "Name": "Corneal dystrophy"
        },
        {
            "DiseaseGroup": "Skeletal disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.44",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Craniosynostosis syndromes",
                "Craniosynostosis syndromes phenotypes",
                "Rare syndromic craniosynostosis or isolated multisuture synostosis"
            ],
            "DiseaseSubGroup": "Craniosynostosis syndromes",
            "CurrentCreated": "2018-12-17T15:47:11.316091Z",
            "Panel_Id": "55b605f722c1fc05fd2345af",
            "Status": "public",
            "Number_of_Regions": 1,
            "Number_of_Genes": 64,
            "Name": "Craniosynostosis"
        },
        {
            "DiseaseGroup": "",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.1",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "",
            "CurrentCreated": "2017-11-05T02:37:19.823394Z",
            "Panel_Id": "5763f3788f620350a199604a",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 11,
            "Name": "Currarino triad"
        },
        {
            "DiseaseGroup": "Renal and urinary tract disorders",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.36",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Cystic kidney disease"
            ],
            "DiseaseSubGroup": "Structural renal and urinary tract disease",
            "CurrentCreated": "2019-01-30T14:18:22.196803Z",
            "Panel_Id": "55a646ef22c1fc6710839b9a",
            "Status": "public",
            "Number_of_Regions": 2,
            "Number_of_Genes": 60,
            "Name": "Cystic kidney disease"
        },
        {
            "DiseaseGroup": "Haematological disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.65",
            "Number_of_STRs": 0,
            "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"
            ],
            "DiseaseSubGroup": "Anaemias and red cell disorders",
            "CurrentCreated": "2017-11-05T02:37:20.141069Z",
            "Panel_Id": "58a70e858f62037e8779b2e8",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 217,
            "Name": "Cytopaenias and congenital anaemias"
        },
        {
            "DiseaseGroup": "Hearing and ear disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.16",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Bilateral microtia",
                "Ear malformations with hearing impairment",
                "Ear malformations",
                "Familial hemifacial microsomia"
            ],
            "DiseaseSubGroup": "Deafness and congenital structural abnormalities",
            "CurrentCreated": "2019-01-28T09:59:52.697275Z",
            "Panel_Id": "57f4dbd18f62036d37cfe4e4",
            "Status": "public",
            "Number_of_Regions": 3,
            "Number_of_Genes": 54,
            "Name": "Deafness and congenital structural abnormalities"
        },
        {
            "DiseaseGroup": "Endocrine disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.24",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Neonatal diabetes (diagnosed less than 6 months)",
                "Neonatal diabetes",
                "Neonatal diabetes diagnosed <6 months"
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