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

{
    "result": [
        {
            "Name": "Adult solid tumours for rare disease",
            "DiseaseSubGroup": "Tumour syndromes",
            "DiseaseGroup": "Tumour syndromes",
            "CurrentVersion": "1.22",
            "CurrentCreated": "2019-06-20T15:10:02.142139Z",
            "Number_of_Genes": 58,
            "Number_of_STRs": 0,
            "Number_of_Regions": 1,
            "Panel_Id": "391",
            "Relevant_disorders": [
                "Young adult onset cancer",
                "Exceptionally young adult onset cancer",
                "Multiple Tumours",
                "Rare tumour predisposition syndromes"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Amelogenesis imperfecta",
            "DiseaseSubGroup": "Skeletal dysplasias",
            "DiseaseGroup": "Skeletal disorders",
            "CurrentVersion": "2.0",
            "CurrentCreated": "2019-09-04T13:55:51.137280Z",
            "Number_of_Genes": 39,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "58c7f3c78f620328d77ce70e",
            "Relevant_disorders": [
                "Amelogenesis Imperfecta",
                "R340"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Amyotrophic lateral sclerosis/motor neuron disease",
            "DiseaseSubGroup": "Neurodegenerative disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.29",
            "CurrentCreated": "2019-06-20T15:14:55.521778Z",
            "Number_of_Genes": 30,
            "Number_of_STRs": 4,
            "Number_of_Regions": 0,
            "Panel_Id": "55d30b0322c1fc2ff2a5bf7b",
            "Relevant_disorders": [
                "Amyotrophic lateral sclerosis or motor neuron disease"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Anophthalmia or microphthalmia",
            "DiseaseSubGroup": "Ocular malformations",
            "DiseaseGroup": "Ophthalmological disorders",
            "CurrentVersion": "1.21",
            "CurrentCreated": "2019-06-20T15:14:55.669056Z",
            "Number_of_Genes": 58,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f97abbb5a1616e5ed45f9",
            "Relevant_disorders": [
                "Anophthalmia or microphthamia",
                "Anophthalmia/microphthamia",
                "Anophthalmia/microphthalmia"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Arrhythmogenic cardiomyopathy",
            "DiseaseSubGroup": "Cardiomyopathy",
            "DiseaseGroup": "Cardiovascular disorders",
            "CurrentVersion": "1.56",
            "CurrentCreated": "2019-12-04T10:00:39.072167Z",
            "Number_of_Genes": 20,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55a3876e22c1fc63fec6d0da",
            "Relevant_disorders": [
                "Arrhythmogenic Right Ventricular Cardiomyopathy",
                "Arrythmogenic cardiomyopathy",
                "R133"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Arthrogryposis",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "2.108",
            "CurrentCreated": "2019-11-29T14:10:03.296394Z",
            "Number_of_Genes": 273,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55b75d5b22c1fc05fd2345c9",
            "Relevant_disorders": [
                "Arthrogrythsis",
                "R83"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Atypical haemolytic uraemic syndrome",
            "DiseaseSubGroup": "Syndromes with prominent renal abnormalities",
            "DiseaseGroup": "Renal and urinary tract disorders",
            "CurrentVersion": "2.1",
            "CurrentCreated": "2019-08-19T11:44:11.988896Z",
            "Number_of_Genes": 13,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "563248da22c1fc58285b283a",
            "Relevant_disorders": [
                "R201"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Auditory Neuropathy Spectrum Disorder",
            "DiseaseSubGroup": "Non-syndromic hearing loss",
            "DiseaseGroup": "Hearing and ear disorders",
            "CurrentVersion": "1.8",
            "CurrentCreated": "2019-02-17T23:29:21.469051Z",
            "Number_of_Genes": 5,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55b20bdf22c1fc7dd6b9bbb7",
            "Relevant_disorders": [
                "Auditory Neuropathy Spectrum Disorder",
                "Auditory Neuropathy Spectrum Disorde"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Autosomal recessive congenital ichthyosis",
            "DiseaseSubGroup": "Ichthyoses",
            "DiseaseGroup": "Dermatological disorders",
            "CurrentVersion": "1.9",
            "CurrentCreated": "2019-06-20T15:14:56.521067Z",
            "Number_of_Genes": 14,
            "Number_of_STRs": 0,
            "Number_of_Regions": 1,
            "Panel_Id": "562e5d2622c1fc582756e3b5",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders",
            "DiseaseSubGroup": "Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders",
            "DiseaseGroup": "Growth disorders",
            "CurrentVersion": "1.92",
            "CurrentCreated": "2019-09-02T14:51:54.105635Z",
            "Number_of_Genes": 22,
            "Number_of_STRs": 0,
            "Number_of_Regions": 1,
            "Panel_Id": "56fa8eb88f62030f36e3026b",
            "Relevant_disorders": [
                "Atypical Beckwith-Wiedemann syndrome",
                "Classical Beckwith-Wiedemann syndrome",
                "Simpson-Golabi-Behmel syndrome",
                "Sotos syndrome",
                "Weaver syndrome"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Brain channelopathy",
            "DiseaseSubGroup": "Channelopathies",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.55",
            "CurrentCreated": "2019-09-09T12:58:28.671278Z",
            "Number_of_Genes": 24,
            "Number_of_STRs": 5,
            "Number_of_Regions": 1,
            "Panel_Id": "55c2321822c1fc0fe5e416e1",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Brugada syndrome",
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "DiseaseGroup": "Cardiovascular disorders",
            "CurrentVersion": "1.46",
            "CurrentCreated": "2019-12-04T10:02:03.095128Z",
            "Number_of_Genes": 23,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55a3a78122c1fc6711b0c6b5",
            "Relevant_disorders": [
                "R128"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "CAKUT",
            "DiseaseSubGroup": "Structural renal and urinary tract disease",
            "DiseaseGroup": "Renal and urinary tract disorders",
            "CurrentVersion": "1.40",
            "CurrentCreated": "2019-11-05T13:52:54.156640Z",
            "Number_of_Genes": 65,
            "Number_of_STRs": 0,
            "Number_of_Regions": 1,
            "Panel_Id": "553f9696bb5a1616e5ed45d1",
            "Relevant_disorders": [
                "Congenital Anomaly of the Kidneys and Urinary Tract (CAKUT)"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Cataracts",
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "DiseaseGroup": "Ophthalmological disorders",
            "CurrentVersion": "2.1",
            "CurrentCreated": "2019-11-11T10:46:00.813551Z",
            "Number_of_Genes": 173,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f979fbb5a1616e5ed45f8",
            "Relevant_disorders": [
                "R31"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Catecholaminergic polymorphic VT",
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "DiseaseGroup": "Cardiovascular disorders",
            "CurrentVersion": "1.26",
            "CurrentCreated": "2019-12-04T10:02:41.354604Z",
            "Number_of_Genes": 10,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55a3aac122c1fc6710839b7d",
            "Relevant_disorders": [
                "Catecholaminergic Polymorphic Ventricular Tachycardia",
                "R129"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Cerebellar hypoplasia",
            "DiseaseSubGroup": "Motor Disorders of the CNS",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.39",
            "CurrentCreated": "2019-10-07T10:30:38.401018Z",
            "Number_of_Genes": 66,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "568f871422c1fc1c79ca176d",
            "Relevant_disorders": [
                "Cerebellar Hypoplasia",
                "Pontine tegmental cap dysplasia"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Cerebral folate deficiency",
            "DiseaseSubGroup": "Specific metabolic abnormalities",
            "DiseaseGroup": "Metabolic disorders",
            "CurrentVersion": "1.2",
            "CurrentCreated": "2017-11-05T02:37:20.047324Z",
            "Number_of_Genes": 4,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55537918bb5a161bf644a3c7",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Cerebral vascular malformations",
            "DiseaseSubGroup": "Cerebrovascular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.70",
            "CurrentCreated": "2019-12-02T17:21:38.053844Z",
            "Number_of_Genes": 100,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "5819a24f8f6203341de99c89",
            "Relevant_disorders": [
                "Cerebrovascular disorders",
                "Vein of Galen malformation",
                "Cerebral arteriovenous malformations",
                "Moyamoya disease",
                "R336"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Choanal atresia",
            "DiseaseSubGroup": "Choanal anomalies",
            "DiseaseGroup": "Skeletal disorders",
            "CurrentVersion": "1.13",
            "CurrentCreated": "2019-06-20T15:10:33.283018Z",
            "Number_of_Genes": 12,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f9697bb5a1616e5ed45d3",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Chondrodysplasia punctata",
            "DiseaseSubGroup": "Skeletal dysplasias",
            "DiseaseGroup": "Skeletal disorders",
            "CurrentVersion": "1.2",
            "CurrentCreated": "2017-11-05T02:37:19.878296Z",
            "Number_of_Genes": 5,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "554a0ac9bb5a167e4ccd1ec0",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Classical tuberous sclerosis",
            "DiseaseSubGroup": "Neurodevelopmental disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.2",
            "CurrentCreated": "2017-11-05T02:37:20.208587Z",
            "Number_of_Genes": 2,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f968cbb5a1616e5ed45cc",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Clefting",
            "DiseaseSubGroup": "Dysmorphic disorders",
            "DiseaseGroup": "Dysmorphic and congenital abnormality syndromes",
            "CurrentVersion": "1.60",
            "CurrentCreated": "2019-11-26T12:11:16.962904Z",
            "Number_of_Genes": 258,
            "Number_of_STRs": 0,
            "Number_of_Regions": 5,
            "Panel_Id": "57acb8268f620364dc61afd3",
            "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"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease-virtual",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital adrenal hypoplasia",
            "DiseaseSubGroup": "Adrenal disorders",
            "DiseaseGroup": "Endocrine disorders",
            "CurrentVersion": "2.0",
            "CurrentCreated": "2019-07-31T14:08:52.172447Z",
            "Number_of_Genes": 20,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55bf785822c1fc0fe45530bf",
            "Relevant_disorders": [
                "R150"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital disorders of glycosylation",
            "DiseaseSubGroup": "Specific metabolic abnormalities",
            "DiseaseGroup": "Metabolic disorders",
            "CurrentVersion": "1.32",
            "CurrentCreated": "2019-10-07T16:15:06.398101Z",
            "Number_of_Genes": 100,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "58346b8b8f62036225ca8a7d",
            "Relevant_disorders": [
                "Congential disorders of glycosylation"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital hyperinsulinism",
            "DiseaseSubGroup": "Disorders of unusual phenotypes",
            "DiseaseGroup": "Endocrine disorders",
            "CurrentVersion": "2.0",
            "CurrentCreated": "2019-07-31T13:49:21.556866Z",
            "Number_of_Genes": 19,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f9781bb5a1616e5ed45f4",
            "Relevant_disorders": [
                "Hyperinsulinism",
                "R144"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital hypothyroidism",
            "DiseaseSubGroup": "Thyroid disorders",
            "DiseaseGroup": "Endocrine disorders",
            "CurrentVersion": "2.0",
            "CurrentCreated": "2019-07-31T13:52:41.584963Z",
            "Number_of_Genes": 34,
            "Number_of_STRs": 0,
            "Number_of_Regions": 2,
            "Panel_Id": "5763f2938f620350a1996046",
            "Relevant_disorders": [
                "Congenital hypothyroidism or thyroid agenesis",
                "R145"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital muscular dystrophy",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.77",
            "CurrentCreated": "2019-12-04T14:37:34.774518Z",
            "Number_of_Genes": 54,
            "Number_of_STRs": 1,
            "Number_of_Regions": 0,
            "Panel_Id": "55b117c022c1fc7dd7ce411c",
            "Relevant_disorders": [
                "R79"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital myaesthenic syndrome",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.75",
            "CurrentCreated": "2019-12-02T11:01:27.788542Z",
            "Number_of_Genes": 35,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f94c2bb5a1616e5ed459c",
            "Relevant_disorders": [
                "Congenital myaesthenia",
                "Congenital myasthenia",
                "R80"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital myopathy",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.234",
            "CurrentCreated": "2019-12-05T16:55:08.416075Z",
            "Number_of_Genes": 108,
            "Number_of_STRs": 2,
            "Number_of_Regions": 3,
            "Panel_Id": "553f94b6bb5a1616e5ed459a",
            "Relevant_disorders": [
                "R81"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Corneal abnormalities",
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "DiseaseGroup": "Ophthalmological disorders",
            "CurrentVersion": "1.7",
            "CurrentCreated": "2019-04-01T14:16:45.925824Z",
            "Number_of_Genes": 42,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f979ebb5a1616e5ed45f6",
            "Relevant_disorders": [
                "Corneal abnormalities",
                "Corneal dystrophy"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Craniosynostosis",
            "DiseaseSubGroup": "Craniosynostosis syndromes",
            "DiseaseGroup": "Skeletal disorders",
            "CurrentVersion": "2.0",
            "CurrentCreated": "2019-09-17T13:00:09.542482Z",
            "Number_of_Genes": 114,
            "Number_of_STRs": 0,
            "Number_of_Regions": 2,
            "Panel_Id": "55b605f722c1fc05fd2345af",
            "Relevant_disorders": [
                "Craniosynostosis syndromes",
                "Craniosynostosis syndromes phenotypes",
                "Rare syndromic craniosynostosis or isolated multisuture synostosis",
                "R100"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Currarino triad",
            "DiseaseSubGroup": "",
            "DiseaseGroup": "",
            "CurrentVersion": "1.1",
            "CurrentCreated": "2017-11-05T02:37:19.823394Z",
            "Number_of_Genes": 11,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "5763f3788f620350a199604a",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Cystic kidney disease",
            "DiseaseSubGroup": "Structural renal and urinary tract disease",
            "DiseaseGroup": "Renal and urinary tract disorders",
            "CurrentVersion": "2.0",
            "CurrentCreated": "2019-09-03T14:24:08.102447Z",
            "Number_of_Genes": 65,
            "Number_of_STRs": 0,
            "Number_of_Regions": 2,
            "Panel_Id": "55a646ef22c1fc6710839b9a",
            "Relevant_disorders": [
                "Cystic kidney disease"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Cytopenias and congenital anaemias",
            "DiseaseSubGroup": "Anaemias and red cell disorders",
            "DiseaseGroup": "Haematological disorders",
            "CurrentVersion": "1.73",
            "CurrentCreated": "2019-09-23T11:25:32.403071Z",
            "Number_of_Genes": 219,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "58a70e858f62037e8779b2e8",
            "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"
            ],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Deafness and congenital structural abnormalities",
            "DiseaseSubGroup": "Deafness and congenital structural abnormalities",
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