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

{
    "result": [
        {
            "Name": "Adult solid tumours for rare disease",
            "DiseaseSubGroup": "Tumour syndromes",
            "DiseaseGroup": "Tumour syndromes",
            "CurrentVersion": "1.40",
            "CurrentCreated": "2024-01-24T18:23:26.818298Z",
            "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": "3.3",
            "CurrentCreated": "2023-10-26T10:36:53.878055Z",
            "Number_of_Genes": 40,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "58c7f3c78f620328d77ce70e",
            "Relevant_disorders": [
                "Amelogenesis Imperfecta",
                "R340"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease",
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Amyotrophic lateral sclerosis/motor neuron disease",
            "DiseaseSubGroup": "Neurodegenerative disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.69",
            "CurrentCreated": "2024-01-24T10:13:10.924246Z",
            "Number_of_Genes": 38,
            "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": "1.51",
            "CurrentCreated": "2022-10-06T21:20:08.139573Z",
            "Number_of_Genes": 63,
            "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 right ventricular cardiomyopathy",
            "DiseaseSubGroup": "Cardiomyopathy",
            "DiseaseGroup": "Cardiovascular disorders",
            "CurrentVersion": "3.9",
            "CurrentCreated": "2023-10-26T00:58:11.438473Z",
            "Number_of_Genes": 20,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55a3876e22c1fc63fec6d0da",
            "Relevant_disorders": [
                "Arrhythmogenic cardiomyopathy",
                "R133"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Arthrogryposis",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "5.31",
            "CurrentCreated": "2024-04-25T09:51:19.458728Z",
            "Number_of_Genes": 298,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55b75d5b22c1fc05fd2345c9",
            "Relevant_disorders": [
                "Arthrogrythsis",
                "R83"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Atypical haemolytic uraemic syndrome",
            "DiseaseSubGroup": "Syndromes with prominent renal abnormalities",
            "DiseaseGroup": "Renal and urinary tract disorders",
            "CurrentVersion": "3.3",
            "CurrentCreated": "2023-10-26T01:24:27.011200Z",
            "Number_of_Genes": 15,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "563248da22c1fc58285b283a",
            "Relevant_disorders": [
                "R201"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease",
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Auditory Neuropathy Spectrum Disorder",
            "DiseaseSubGroup": "Non-syndromic hearing loss",
            "DiseaseGroup": "Hearing and ear disorders",
            "CurrentVersion": "1.9",
            "CurrentCreated": "2022-04-12T14:45:11.338706Z",
            "Number_of_Genes": 8,
            "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": "1.14",
            "CurrentCreated": "2022-03-16T10:03:33.804804Z",
            "Number_of_Genes": 15,
            "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": "1.120",
            "CurrentCreated": "2023-08-09T11:26:35.704386Z",
            "Number_of_Genes": 30,
            "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": "Bilateral congenital or childhood onset cataracts",
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "DiseaseGroup": "Ophthalmological disorders",
            "CurrentVersion": "4.12",
            "CurrentCreated": "2024-04-15T16:01:59.571391Z",
            "Number_of_Genes": 201,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f979fbb5a1616e5ed45f8",
            "Relevant_disorders": [
                "Cataracts",
                "R31"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Brain channelopathy",
            "DiseaseSubGroup": "Channelopathies",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.80",
            "CurrentCreated": "2022-09-13T11:25:47.802810Z",
            "Number_of_Genes": 26,
            "Number_of_STRs": 5,
            "Number_of_Regions": 1,
            "Panel_Id": "55c2321822c1fc0fe5e416e1",
            "Relevant_disorders": [],
            "Status": "public",
            "PanelTypes": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Brugada syndrome and cardiac sodium channel disease",
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "DiseaseGroup": "Cardiovascular disorders",
            "CurrentVersion": "3.8",
            "CurrentCreated": "2024-01-22T16:17:26.552961Z",
            "Number_of_Genes": 23,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "55a3a78122c1fc6711b0c6b5",
            "Relevant_disorders": [
                "Brugada syndrome",
                "R128"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "CAKUT",
            "DiseaseSubGroup": "Structural renal and urinary tract disease",
            "DiseaseGroup": "Renal and urinary tract disorders",
            "CurrentVersion": "1.176",
            "CurrentCreated": "2024-04-23T11:38:43.467410Z",
            "Number_of_Genes": 101,
            "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": [
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Catecholaminergic polymorphic VT",
            "DiseaseSubGroup": "Cardiac arrhythmia",
            "DiseaseGroup": "Cardiovascular disorders",
            "CurrentVersion": "4.4",
            "CurrentCreated": "2023-10-26T00:55:59.423692Z",
            "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",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Cerebellar hypoplasia",
            "DiseaseSubGroup": "Motor Disorders of the CNS",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "1.73",
            "CurrentCreated": "2023-05-30T11:34:18.926106Z",
            "Number_of_Genes": 76,
            "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": "3.16",
            "CurrentCreated": "2024-04-24T16:23:20.959409Z",
            "Number_of_Genes": 105,
            "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",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Childhood solid tumours",
            "DiseaseSubGroup": "Childhood Tumours",
            "DiseaseGroup": "Tumour syndromes",
            "CurrentVersion": "4.18",
            "CurrentCreated": "2024-04-11T12:52:20.613240Z",
            "Number_of_Genes": 121,
            "Number_of_STRs": 0,
            "Number_of_Regions": 1,
            "Panel_Id": "55af539322c1fc78a9ef5052",
            "Relevant_disorders": [
                "Paediatric congenital malformation-dysmorphism-tumour syndrome",
                "Paediatric congenital malformation-dysmorphism-tumour syndromes",
                "Paediatric congenital malformation-dysmorphism-tumour sydromes",
                "Paediatric congenital malformation-dysmorphism-tumour syndrome",
                "Tumour predisposition - childhood onset",
                "R359"
            ],
            "Status": "public",
            "PanelTypes": [
                "gms-cancer-germline-virtual",
                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Choanal atresia",
            "DiseaseSubGroup": "Choanal anomalies",
            "DiseaseGroup": "Skeletal disorders",
            "CurrentVersion": "1.16",
            "CurrentCreated": "2022-02-14T11:23:27.044303Z",
            "Number_of_Genes": 14,
            "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": "1.5",
            "CurrentCreated": "2021-09-07T14:17:08.166044Z",
            "Number_of_Genes": 6,
            "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": "4.110",
            "CurrentCreated": "2024-04-24T15:59:12.897324Z",
            "Number_of_Genes": 306,
            "Number_of_STRs": 0,
            "Number_of_Regions": 6,
            "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",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital adrenal hypoplasia",
            "DiseaseSubGroup": "Adrenal disorders",
            "DiseaseGroup": "Endocrine disorders",
            "CurrentVersion": "3.11",
            "CurrentCreated": "2024-04-10T19:07:17.272874Z",
            "Number_of_Genes": 23,
            "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": "4.18",
            "CurrentCreated": "2024-01-31T18:03:30.344768Z",
            "Number_of_Genes": 117,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "58346b8b8f62036225ca8a7d",
            "Relevant_disorders": [
                "Congential disorders of glycosylation"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital hyperinsulinism",
            "DiseaseSubGroup": "Disorders of unusual phenotypes",
            "DiseaseGroup": "Endocrine disorders",
            "CurrentVersion": "3.4",
            "CurrentCreated": "2023-10-26T01:03:07.711656Z",
            "Number_of_Genes": 24,
            "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": "2.18",
            "CurrentCreated": "2023-11-30T12:12:27.487017Z",
            "Number_of_Genes": 35,
            "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": "4.23",
            "CurrentCreated": "2024-02-20T14:20:15.924380Z",
            "Number_of_Genes": 60,
            "Number_of_STRs": 1,
            "Number_of_Regions": 0,
            "Panel_Id": "55b117c022c1fc7dd7ce411c",
            "Relevant_disorders": [
                "R79"
            ],
            "Status": "public",
            "PanelTypes": [
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                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital myaesthenic syndrome",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "4.5",
            "CurrentCreated": "2023-10-25T21:08:55.767856Z",
            "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",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Congenital myopathy",
            "DiseaseSubGroup": "Neuromuscular disorders",
            "DiseaseGroup": "Neurology and neurodevelopmental disorders",
            "CurrentVersion": "4.37",
            "CurrentCreated": "2024-04-03T11:24:42.434877Z",
            "Number_of_Genes": 124,
            "Number_of_STRs": 2,
            "Number_of_Regions": 3,
            "Panel_Id": "553f94b6bb5a1616e5ed459a",
            "Relevant_disorders": [
                "R81"
            ],
            "Status": "public",
            "PanelTypes": [
                "component-of-super-panel",
                "gms-rare-disease",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        },
        {
            "Name": "Corneal abnormalities",
            "DiseaseSubGroup": "Anterior segment abnormalities",
            "DiseaseGroup": "Ophthalmological disorders",
            "CurrentVersion": "1.13",
            "CurrentCreated": "2024-01-07T20:09:15.005884Z",
            "Number_of_Genes": 43,
            "Number_of_STRs": 0,
            "Number_of_Regions": 0,
            "Panel_Id": "553f979ebb5a1616e5ed45f6",
            "Relevant_disorders": [
                "Corneal abnormalities",
                "Corneal dystrophy"
            ],
            "Status": "public",
            "PanelTypes": [
                "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": "4.24",
            "CurrentCreated": "2024-01-02T13:34:19.183239Z",
            "Number_of_Genes": 73,
            "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": "1.118",
            "CurrentCreated": "2024-03-12T16:43:58.905273Z",
            "Number_of_Genes": 223,
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                "gms-rare-disease-virtual",
                "gms-signed-off",
                "rare-disease-100k"
            ]
        }
    ]
}