{"count":220790,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1983","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&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"}]}