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": "1.14",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Amelogenesis Imperfecta"
            ],
            "DiseaseSubGroup": "Skeletal dysplasias",
            "CurrentCreated": "2019-06-11T10:42:00.153343Z",
            "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": "1.27",
            "Number_of_STRs": 4,
            "Relevant_disorders": [
                "Amyotrophic lateral sclerosis or motor neuron disease"
            ],
            "DiseaseSubGroup": "Neurodegenerative disorders",
            "CurrentCreated": "2019-06-11T17:03:06.706591Z",
            "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": 58,
            "Name": "Anophthalmia or microphthalmia"
        },
        {
            "DiseaseGroup": "Cardiovascular disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.23",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Arrhythmogenic Right Ventricular Cardiomyopathy",
                "Arrythmogenic cardiomyopathy"
            ],
            "DiseaseSubGroup": "Cardiomyopathy",
            "CurrentCreated": "2019-03-25T16:30:32.499128Z",
            "Panel_Id": "55a3876e22c1fc63fec6d0da",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 18,
            "Name": "Arrhythmogenic cardiomyopathy"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "2.41",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Arthrogrythsis"
            ],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2019-05-03T16:46:08.796421Z",
            "Panel_Id": "55b75d5b22c1fc05fd2345c9",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 246,
            "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": "1.8",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Auditory Neuropathy Spectrum Disorder",
                "Auditory Neuropathy Spectrum Disorde"
            ],
            "DiseaseSubGroup": "Non-syndromic hearing loss",
            "CurrentCreated": "2019-02-17T23:29:21.469051Z",
            "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": "1.90",
            "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": "2019-05-31T11:17:01.091929Z",
            "Panel_Id": "56fa8eb88f62030f36e3026b",
            "Status": "public",
            "Number_of_Regions": 1,
            "Number_of_Genes": 22,
            "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": "1.39",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "CurrentCreated": "2019-03-25T17:17:59.747092Z",
            "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": "1.37",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Congenital Anomaly of the Kidneys and Urinary Tract (CAKUT)"
            ],
            "DiseaseSubGroup": "Structural renal and urinary tract disease",
            "CurrentCreated": "2019-06-03T10:45:14.576146Z",
            "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": "1.26",
            "Number_of_STRs": 0,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "CurrentCreated": "2019-02-19T10:51:30.380661Z",
            "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": "1.14",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Catecholaminergic Polymorphic Ventricular Tachycardia"
            ],
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "CurrentCreated": "2019-03-25T17:20:35.501732Z",
            "Panel_Id": "55a3aac122c1fc6710839b7d",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 10,
            "Name": "Catecholaminergic polymorphic VT"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.34",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Cerebellar Hypoplasia",
                "Pontine tegmental cap dysplasia"
            ],
            "DiseaseSubGroup": "Motor Disorders of the CNS",
            "CurrentCreated": "2019-05-16T09:21:41.810674Z",
            "Panel_Id": "568f871422c1fc1c79ca176d",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 65,
            "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": 95,
            "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": "1.37",
            "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": "2019-06-12T16:48:43.607074Z",
            "Panel_Id": "57acb8268f620364dc61afd3",
            "Status": "public",
            "Number_of_Regions": 5,
            "Number_of_Genes": 253,
            "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": "1.24",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Congential disorders of glycosylation"
            ],
            "DiseaseSubGroup": "Specific metabolic abnormalities",
            "CurrentCreated": "2019-02-18T15:21:48.987946Z",
            "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": "1.47",
            "Number_of_STRs": 1,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2019-05-03T12:55:09.298250Z",
            "Panel_Id": "55b117c022c1fc7dd7ce411c",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 53,
            "Name": "Congenital muscular dystrophy"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.47",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Congenital myaesthenia",
                "Congenital myasthenia"
            ],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2019-05-10T11:16:45.814712Z",
            "Panel_Id": "553f94c2bb5a1616e5ed459c",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 35,
            "Name": "Congenital myaesthenic syndrome"
        },
        {
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "PanelTypes": [
                "gms-rare-disease",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.149",
            "Number_of_STRs": 2,
            "Relevant_disorders": [],
            "DiseaseSubGroup": "Neuromuscular disorders",
            "CurrentCreated": "2019-05-04T13:03:41.250756Z",
            "Panel_Id": "553f94b6bb5a1616e5ed459a",
            "Status": "public",
            "Number_of_Regions": 3,
            "Number_of_Genes": 99,
            "Name": "Congenital myopathy"
        },
        {
            "DiseaseGroup": "Ophthalmological disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.7",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Corneal abnormalities",
                "Corneal dystrophy"
            ],
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "CurrentCreated": "2019-04-01T14:16:45.925824Z",
            "Panel_Id": "553f979ebb5a1616e5ed45f6",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 42,
            "Name": "Corneal abnormalities"
        },
        {
            "DiseaseGroup": "Skeletal disorders",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.122",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Craniosynostosis syndromes",
                "Craniosynostosis syndromes phenotypes",
                "Rare syndromic craniosynostosis or isolated multisuture synostosis"
            ],
            "DiseaseSubGroup": "Craniosynostosis syndromes",
            "CurrentCreated": "2019-06-11T13:11:15.792959Z",
            "Panel_Id": "55b605f722c1fc05fd2345af",
            "Status": "public",
            "Number_of_Regions": 2,
            "Number_of_Genes": 113,
            "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": "1.44",
            "Number_of_STRs": 0,
            "Relevant_disorders": [
                "Cystic kidney disease"
            ],
            "DiseaseSubGroup": "Structural renal and urinary tract disease",
            "CurrentCreated": "2019-03-28T14:17:18.013743Z",
            "Panel_Id": "55a646ef22c1fc6710839b9a",
            "Status": "public",
            "Number_of_Regions": 2,
            "Number_of_Genes": 62,
            "Name": "Cystic kidney disease"
        },
        {
            "DiseaseGroup": "Haematological disorders",
            "PanelTypes": [
                "rare-disease-100k"
            ],
            "CurrentVersion": "1.69",
            "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",
                "Cytopaenias and congenital anaemias",
                "Cytopenia and pancytopenia"
            ],
            "DiseaseSubGroup": "Anaemias and red cell disorders",
            "CurrentCreated": "2019-04-01T16:01:09.391389Z",
            "Panel_Id": "58a70e858f62037e8779b2e8",
            "Status": "public",
            "Number_of_Regions": 0,
            "Number_of_Genes": 218,
            "Name": "Cytopenias 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)",
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