HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220790,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1983",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1981",
"results": [
{
"created": "2020-01-15T15:31:04.677796+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Long QT syndrome_VCGS to Long QT Syndrome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:29:32.378107+11:00",
"panel_name": "Lissencephaly and band heterotopia",
"panel_id": 15,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Lissencephaly and band heterotopia_AustralianGenomics_VCGS to Lissencephaly and band heterotopia\nPanel types changed to Victorian Clinical Genetics Services; Australian Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:28:58.699957+11:00",
"panel_name": "Lipodystrophy_Lipoatrophy",
"panel_id": 130,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Lipodystrophy / Lipoatrophy_VCGS to Lipodystrophy_Lipoatrophy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:25:21.851361+11:00",
"panel_name": "Kidneyome_SuperPanel",
"panel_id": 275,
"panel_version": "0.241",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Kidneyome_SuperPanel_KidGen_VCGS to Kidneyome_SuperPanel\nPanel types changed to Superpanel; Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:25:02.425585+11:00",
"panel_name": "Kabuki syndrome",
"panel_id": 134,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Kabuki syndrome_VCGS to Kabuki syndrome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:24:07.090656+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations",
"panel_id": 129,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Joubert syndrome and other cerebellar malformations_VCGS to Joubert syndrome and other cerebellar malformations\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:22:55.801097+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1595",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Intellectual disability, syndromic and non-syndromic_GHQ_VCGS to Intellectual disability, syndromic and non-syndromic\nPanel types changed to Genetic Health Queensland; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:22:34.866243+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Inflammatory bowel disease_VCGS to Inflammatory bowel disease\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:21:29.990699+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Incidentalome_VCGS to Incidentalome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:20:19.495557+11:00",
"panel_name": "Immunological disorders_SuperPanel",
"panel_id": 239,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Immunological disorders_SuperPanel_VCGS to Immunological disorders_SuperPanel\nPanel types changed to Superpanel; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:19:41.672534+11:00",
"panel_name": "Ichthyosis",
"panel_id": 124,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Ichthyosis_VCGS to Ichthyosis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:19:18.028149+11:00",
"panel_name": "Hypophosphataemic Rickets",
"panel_id": 122,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hypophosphataemic Rickets_VCGS to Hypophosphataemic Rickets\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:18:05.087612+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hypertrophic cardiomyopathy_VCGS to Hypertrophic cardiomyopathy_HCM\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:16:50.892925+11:00",
"panel_name": "Hypertrichosis syndromes",
"panel_id": 120,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hypertrichosis syndromes_VCGS to Hypertrichosis syndromes\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:15:21.277501+11:00",
"panel_name": "Hyperinsulinism",
"panel_id": 118,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hyperinsulinism_VCGS to Hyperinsulinism\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:14:08.606934+11:00",
"panel_name": "Hypercalcaemia",
"panel_id": 117,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hypercalcaemia_VCGS to Hypercalcaemia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:13:52.927707+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hydrops fetalis_VCGS to Hydrops fetalis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:12:59.824677+11:00",
"panel_name": "Hydrocephalus_Ventriculomegaly",
"panel_id": 115,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hydrocephalus/Ventriculomegaly_VCGS to Hydrocephalus_Ventriculomegaly\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:12:35.691842+11:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Holoprosencephaly and septo-optic dysplasia_VCGS to Holoprosencephaly and septo-optic dysplasia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:11:56.302194+11:00",
"panel_name": "Hirschsprung disease",
"panel_id": 110,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hirschsprung disease_VCGS to Hirschsprung disease\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:10:55.448440+11:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Heterotaxy_VCGS to Heterotaxy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:10:02.984041+11:00",
"panel_name": "Hereditary angioedema",
"panel_id": 226,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hereditary angioedema_MelbourneGenomics_VCGS to Hereditary angioedema\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:05:55.474751+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: EXOSC8 as ready",
"entity_name": "EXOSC8",
"entity_type": "gene"
},
{
"created": "2020-01-15T15:05:55.463452+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: exosc8 has been classified as Red List (Low Evidence).",
"entity_name": "EXOSC8",
"entity_type": "gene"
},
{
"created": "2020-01-15T15:05:50.902911+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: EXOSC8 as Red List (low evidence)",
"entity_name": "EXOSC8",
"entity_type": "gene"
},
{
"created": "2020-01-15T15:05:50.895726+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: exosc8 has been classified as Red List (Low Evidence).",
"entity_name": "EXOSC8",
"entity_type": "gene"
},
{
"created": "2020-01-15T15:05:38.182883+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.2",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "reviewed gene: EXOSC8: Rating: RED; Mode of pathogenicity: None; Publications: 24989451; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EXOSC8",
"entity_type": "gene"
},
{
"created": "2020-01-15T14:58:56.277185+11:00",
"panel_name": "Haematuria",
"panel_id": 39,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Haematuria_VCGS_KidGen to Haematuria\nPanel types changed to Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:57:52.311533+11:00",
"panel_name": "Glycogen Storage Diseases",
"panel_id": 106,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Glycogen Storage Diseases_VCGS to Glycogen Storage Diseases\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:57:04.947877+11:00",
"panel_name": "Glaucoma congenital",
"panel_id": 105,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Glaucoma congenital_VCGS to Glaucoma congenital\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:56:43.675519+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.184",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Genetic Epilepsy_AustralianGenomics_VCGS to Genetic Epilepsy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:55:12.925718+11:00",
"panel_name": "Frontonasal dysplasia",
"panel_id": 104,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Frontonasal dysplasia_VCGS to Frontonasal dysplasia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:54:50.202764+11:00",
"panel_name": "Fatty Oxidation Defects",
"panel_id": 103,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Fatty Oxidation Defects_VCGS to Fatty Oxidation Defects\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:54:17.672603+11:00",
"panel_name": "Familial hypercholesterolaemia",
"panel_id": 333,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Familial hypercholesterolaemia_VCGS to Familial hypercholesterolaemia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:53:48.660361+11:00",
"panel_name": "Eye Anterior Segment Abnormalities",
"panel_id": 43,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Eye Anterior Segment Abnormalities_VCGS to Eye Anterior Segment Abnormalities\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:53:08.402472+11:00",
"panel_name": "Epidermolysis bullosa",
"panel_id": 101,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Epidermolysis bullosa_VCGS to Epidermolysis bullosa\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:52:11.691081+11:00",
"panel_name": "Early onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Early onset Parkinson disease_MelbourneGenomics_VCGS to Early onset Parkinson disease\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:51:18.219573+11:00",
"panel_name": "Early-onset Dementia",
"panel_id": 24,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Early-onset Dementia_MGHA_VCGS to Early-onset Dementia\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:49:17.995554+11:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Disorders of Sex Differentiation_VCGS to Disorders of Sex Differentiation\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:49:02.874141+11:00",
"panel_name": "Disorders of immune dysregulation",
"panel_id": 229,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Disorders of immune dysregulation_MelbourneGenomics_VCGS to Disorders of immune dysregulation\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:48:23.187315+11:00",
"panel_name": "Dilated cardiomyopathy_DCM",
"panel_id": 95,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Dilated cardiomyopathy_VCGS to Dilated cardiomyopathy_DCM\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:47:02.537522+11:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Diamond Blackfan anaemia_VCGS to Diamond Blackfan anaemia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:46:14.899139+11:00",
"panel_name": "Desmosomal disorders",
"panel_id": 97,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Desmosomal disorders_VCGS to Desmosomal disorders\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:45:06.332960+11:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Defects of innate immunity_MelbourneGenomics_VCGS to Defects of innate immunity\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:44:17.013849+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.230",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Deafness_MelbourneGenomics_VCGS to Deafness\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:43:37.694847+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Craniosynostosis_VCGS to Craniosynostosis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:43:03.911678+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Corneal Dystrophy_VCGS to Corneal Dystrophy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:40:44.905196+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Congenital Heart Defect_VCGS to Congenital Heart Defect\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:40:03.659601+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Congenital Disorders of Glycosylation_VCGS to Congenital Disorders of Glycosylation\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:39:06.103288+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Congenital Diarrhoea_VCGS to Congenital Diarrhoea\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:38:42.212239+11:00",
"panel_name": "Congenital diaphragmatic hernia",
"panel_id": 69,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Congenital diaphragmatic hernia, CDH_VCGS to Congenital diaphragmatic hernia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:37:12.865653+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:27:53.877590+11:00",
"panel_name": "Complement deficiencies",
"panel_id": 224,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Complement deficiencies_MelbourneGenomics_VCGS to Complement deficiencies\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:26:58.342434+11:00",
"panel_name": "Combined immunodeficiency",
"panel_id": 223,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Combined immunodeficiency_MelbourneGenomics_VCGS to Combined immunodeficiency\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:26:29.722951+11:00",
"panel_name": "Cobblestone malformations",
"panel_id": 6,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cobblestone malformations_AustralianGenomics to Cobblestone malformations\nPanel types changed to Victorian Clinical Genetics Services; Australian Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:24:11.723233+11:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Ciliopathies_VCGS to Ciliopathies\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:23:37.463470+11:00",
"panel_name": "Ciliary dyskinesia",
"panel_id": 82,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Ciliary dyskinesia_VCGS to Ciliary dyskinesia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:22:38.345209+11:00",
"panel_name": "Chromosome breakage disorders",
"panel_id": 79,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Chromosome breakage disorders_VCGS to Chromosome breakage disorders\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:21:18.759518+11:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cholestasis_VCGS to Cholestasis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:17:36.283749+11:00",
"panel_name": "Channelopathy",
"panel_id": 74,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Channelopathy_VCGS to Channelopathy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:16:27.054085+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cerebral Palsy_VCGS to Cerebral Palsy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:15:42.184546+11:00",
"panel_name": "Cerebellar and Pontocerebellar hypoplasia",
"panel_id": 72,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cerebellar and Pontocerebellar hypoplasia_VCGS to Cerebellar and Pontocerebellar hypoplasia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:15:22.985689+11:00",
"panel_name": "Central Hypoventilation",
"panel_id": 71,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Central Hypoventilation_VCGS to Central Hypoventilation\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:14:40.560474+11:00",
"panel_name": "Catecholaminergic polymorphic ventricular tachycardia_CPVT",
"panel_id": 92,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Catecholaminergic polymorphic ventricular tachycardia (CPVT)_VCGS to Catecholaminergic polymorphic ventricular tachycardia_CPVT\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:13:15.951560+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cataract_VCGS to Cataract\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:12:04.742076+11:00",
"panel_name": "Cardiomyopathy_SuperPanel",
"panel_id": 253,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cardiomyopathy_SuperPanel_VCGS to Cardiomyopathy_SuperPanel\nPanel types changed to Superpanel; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:11:58.235162+11:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cancer Predisposition_Paediatric_VCGS to Cancer Predisposition_Paediatric\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:11:10.812109+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Callosome_VCGS to Callosome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:10:42.731255+11:00",
"panel_name": "Brugada syndrome_VCGS",
"panel_id": 60,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:08:08.206795+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.2",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: ASCC1 as ready",
"entity_name": "ASCC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T14:08:07.574164+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.2",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: ascc1 has been classified as Red List (Low Evidence).",
"entity_name": "ASCC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T14:08:00.302222+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.2",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: ASCC1 were set to ",
"entity_name": "ASCC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T14:07:29.079153+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.1",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: ASCC1 as Red List (low evidence)",
"entity_name": "ASCC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T14:07:29.073632+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.1",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Not relevant for testing in an adult hospital. Onset of disease is prenatal and death occurs in the first days or months of life.",
"entity_name": "ASCC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T14:07:29.027286+11:00",
"panel_name": "Hereditary Neuropathy - complex_RMH",
"panel_id": 3070,
"panel_version": "0.1",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: ascc1 has been classified as Red List (Low Evidence).",
"entity_name": "ASCC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T14:07:26.380872+11:00",
"panel_name": "Brain calcification",
"panel_id": 58,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Brain calcification_VCGS to Brain calcification\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:06:30.129488+11:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Bone Marrow Failure_VCGS to Bone Marrow Failure\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:05:36.875420+11:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Blepharophimosis_VCGS to Blepharophimosis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:03:32.769837+11:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Bleeding Disorders_VCGS to Bleeding Disorders\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T14:00:41.135734+11:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Bardet Biedl syndrome_VCGS to Bardet Biedl syndrome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:54:04.018883+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Autism_VCGS to Autism\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:52:52.192360+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN",
"panel_id": 211,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH to Atypical Haemolytic Uraemic Syndrome_MPGN\nPanel types changed to Victorian Clinical Genetics Services; KidGen; Royal Melbourne Hospital",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:51:40.006409+11:00",
"panel_name": "Atrial fibrillation",
"panel_id": 210,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Atrial fibrilation_VCGS to Atrial fibrillation\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:45:34.527766+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Arthrogryposis_VCGS to Arthrogryposis",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:45:33.516115+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Arthrogryposis_VCGS to Arthrogryposis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:41:40.134794+11:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.7",
"user_name": "Sebastian Lunke",
"item_type": "panel",
"text": "Panel name changed from Susceptibility to viral infections_MelbourneGenomics_VCGS to Susceptibility to Viral Infections\nPanel types changed to Melbourne Genomics; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:39:23.222509+11:00",
"panel_name": "Arrhythmogenic right ventricular cardiomyopathy_ARVC",
"panel_id": 48,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Arrhythmogenic right ventricular cardiomyopathy_VCGS to Arrhythmogenic right ventricular cardiomyopathy_ARVC\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:35:29.169755+11:00",
"panel_name": "Arrhythmia_SuperPanel",
"panel_id": 254,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Arrhythmia_SuperPanel_VCGS to Arrhythmia_SuperPanel\nPanel types changed to Superpanel; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:34:51.598387+11:00",
"panel_name": "Aortopathy_Connective tissue disorders",
"panel_id": 44,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Aortopathy, Connective tissue disorder_VCGS to Aortopathy_Connective tissue disorders\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:27:58.517250+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Anophthalmia, microphthalmia, coloboma_VCGS to Anophthalmia_Microphthalmia_Coloboma\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:26:57.300301+11:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Angelman Rett like syndromes_VCGS to Angelman Rett like syndromes\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:25:47.803689+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine",
"panel_id": 40,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Alternating hemiplegia including hemiplegic migraine_VCGS to Alternating hemiplegia including hemiplegic migraine\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:16:06.757481+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.10",
"user_name": "Sebastian Lunke",
"item_type": "panel",
"text": "Panel name changed from Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_VCGS to Systemic Autoinflammatory Disease_Periodic Fever\nPanel types changed to Melbourne Genomics; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:15:13.259955+11:00",
"panel_name": "Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly",
"panel_id": 20,
"panel_version": "0.1",
"user_name": "Sebastian Lunke",
"item_type": "panel",
"text": "Panel name changed from Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS to Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly\nPanel types changed to Australian Genomics; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:12:31.355165+11:00",
"panel_name": "Tubulinopathies",
"panel_id": 21,
"panel_version": "0.1",
"user_name": "Sebastian Lunke",
"item_type": "panel",
"text": "Panel name changed from Tubulinopathies_AustralianGenomics_VCGS to Tubulinopathies\nPanel types changed to Australian Genomics; Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:11:32.417389+11:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Alagille syndrome_VCGS to Alagille syndrome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T13:10:08.716763+11:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Additional findings_Adult_MelbGenomics to Additional findings_Adult\nPanel types changed to Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T12:48:02.786896+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1594",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TEMN3-AS1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T12:01:04.883843+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1593",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "Classified gene: HK1 as Green List (high evidence)",
"entity_name": "HK1",
"entity_type": "gene"
},
{
"created": "2020-01-15T12:01:04.871554+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1593",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "Gene: hk1 has been classified as Green List (High Evidence).",
"entity_name": "HK1",
"entity_type": "gene"
}
]
}