{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=529","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=527","results":[{"created":"2023-11-02T17:02:53.571277+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome 17, 615994 (3) for gene: LZTFL1","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2023-11-02T17:02:52.200997+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Chediak-Higashi syndrome, 214500 (3) for gene: LYST","entity_name":"LYST","entity_type":"gene"},{"created":"2023-11-02T17:02:51.175064+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leigh syndrome, French-Canadian type, 220111 (3) for gene: LRPPRC","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2023-11-02T17:02:49.816251+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Donnai-Barrow syndrome, 222448 (3) for gene: LRP2","entity_name":"LRP2","entity_type":"gene"},{"created":"2023-11-02T17:02:48.487832+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leber congenital amaurosis 14, 613341 (3) for gene: LRAT","entity_name":"LRAT","entity_type":"gene"},{"created":"2023-11-02T17:02:47.186390+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Lipoprotein lipase deficiency, 238600 (3) for gene: LPL","entity_name":"LPL","entity_type":"gene"},{"created":"2023-11-02T17:02:46.363283+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Restrictive dermopathy, lethal, 275210 (3) for gene: LMNA\nPublications for gene LMNA were updated from 18551513; 15148145; 17377071 to 15148145; 18551513; 17377071","entity_name":"LMNA","entity_type":"gene"},{"created":"2023-11-02T17:02:44.963300+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Methylmalonic aciduria and homocystinuria, cblF type, 277380 (3) for gene: LMBRD1","entity_name":"LMBRD1","entity_type":"gene"},{"created":"2023-11-02T17:02:43.669637+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cholesteryl ester storage disease, 278000 (3) for gene: LIPA","entity_name":"LIPA","entity_type":"gene"},{"created":"2023-11-02T17:02:42.707333+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes LIG4 syndrome, 606593 (3) for gene: LIG4","entity_name":"LIG4","entity_type":"gene"},{"created":"2023-11-02T17:02:41.303600+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, 601559 (3) for gene: LIFR","entity_name":"LIFR","entity_type":"gene"},{"created":"2023-11-02T17:02:39.998864+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pituitary hormone deficiency, combined, 3, 221750 (3) for gene: LHX3","entity_name":"LHX3","entity_type":"gene"},{"created":"2023-11-02T17:02:38.706290+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hypercholesterolemia, familial, autosomal recessive, 603813 (3) for gene: LDLRAP1","entity_name":"LDLRAP1","entity_type":"gene"},{"created":"2023-11-02T17:02:37.688376+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes LDL cholesterol level QTL2/Hypercholesterolemia, familial for gene: LDLR","entity_name":"LDLR","entity_type":"gene"},{"created":"2023-11-02T17:02:36.385644+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leber congenital amaurosis 5, 604537 (3) for gene: LCA5","entity_name":"LCA5","entity_type":"gene"},{"created":"2023-11-02T17:02:35.090970+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Infantile liver failure syndrome 1, MIM# 615438 for gene: LARS","entity_name":"LARS","entity_type":"gene"},{"created":"2023-11-02T17:02:34.168210+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6, 613154 (3) for gene: LARGE1","entity_name":"LARGE1","entity_type":"gene"},{"created":"2023-11-02T17:02:32.888165+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa, junctional, Herlitz type, 226700 (3) for gene: LAMC2","entity_name":"LAMC2","entity_type":"gene"},{"created":"2023-11-02T17:02:31.672207+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa, junctional, Herlitz type, 226700 (3) for gene: LAMB3","entity_name":"LAMB3","entity_type":"gene"},{"created":"2023-11-02T17:02:30.395267+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pierson syndrome, 609049 (3) for gene: LAMB2","entity_name":"LAMB2","entity_type":"gene"},{"created":"2023-11-02T17:02:29.465791+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Lissencephaly 5, 615191 (3) for gene: LAMB1","entity_name":"LAMB1","entity_type":"gene"},{"created":"2023-11-02T17:02:28.265260+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa, junctional, Herlitz type, 226700 (3) for gene: LAMA3","entity_name":"LAMA3","entity_type":"gene"},{"created":"2023-11-02T17:02:26.986375+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy, congenital merosin-deficient, 607855 (3) for gene: LAMA2","entity_name":"LAMA2","entity_type":"gene"},{"created":"2023-11-02T17:02:26.072598+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes L-2-hydroxyglutaric aciduria, 236792 (3) for gene: L2HGDH","entity_name":"L2HGDH","entity_type":"gene"},{"created":"2023-11-02T17:02:24.871904+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes MASA syndrome, 303350 (3) for gene: L1CAM","entity_name":"L1CAM","entity_type":"gene"},{"created":"2023-11-02T17:02:23.566781+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa simplex, recessive 1, 601001 (3) for gene: KRT14","entity_name":"KRT14","entity_type":"gene"},{"created":"2023-11-02T17:02:22.268965+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hydrolethalus syndrome 2, 614120 (3) for gene: KIF7","entity_name":"KIF7","entity_type":"gene"},{"created":"2023-11-02T17:02:21.272558+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Spastic paraplegia 30, autosomal recessive, 610357 (3) for gene: KIF1A","entity_name":"KIF1A","entity_type":"gene"},{"created":"2023-11-02T17:02:19.963338+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mental retardation, X-linked, syndromic, Claes-Jensen type, 300534 (3) for gene: KDM5C","entity_name":"KDM5C","entity_type":"gene"},{"created":"2023-11-02T17:02:18.593927+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Jervell and Lange-Nielsen syndrome, 220400 (3) for gene: KCNQ1\nPublications for gene KCNQ1 were updated from 29033053; 28438721 to 29033053; 28438721","entity_name":"KCNQ1","entity_type":"gene"},{"created":"2023-11-02T17:02:17.276015+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hyperinsulinemic hypoglycemia, familial, 2, 601820 (3) for gene: KCNJ11","entity_name":"KCNJ11","entity_type":"gene"},{"created":"2023-11-02T17:02:16.321657+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Bartter syndrome, type 2, 241200 (3) for gene: KCNJ1","entity_name":"KCNJ1","entity_type":"gene"},{"created":"2023-11-02T17:02:14.768470+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Lissencephaly 6, with microcephaly, 616212 (3) for gene: KATNB1","entity_name":"KATNB1","entity_type":"gene"},{"created":"2023-11-02T17:02:13.375711+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes SCID, autosomal recessive, T-negative/B-positive type, 600802 (3) for gene: JAK3","entity_name":"JAK3","entity_type":"gene"},{"created":"2023-11-02T17:02:12.402941+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Isovaleric acidemia, 243500 (3) for gene: IVD","entity_name":"IVD","entity_type":"gene"},{"created":"2023-11-02T17:02:11.132040+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Gillespie syndrome, 206700 (3), Autosomal recessive for gene: ITPR1","entity_name":"ITPR1","entity_type":"gene"},{"created":"2023-11-02T17:02:09.867855+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa, junctional, with pyloric atresia, 226730 (3) for gene: ITGB4","entity_name":"ITGB4","entity_type":"gene"},{"created":"2023-11-02T17:02:08.568885+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa, junctional, with pyloric stenosis, 226730 (3) for gene: ITGA6\nPublications for gene ITGA6 were updated from 31502654; 27607025; 9158140; 34525201; 20301336 to 9158140; 20301336; 27607025; 34525201; 31502654","entity_name":"ITGA6","entity_type":"gene"},{"created":"2023-11-02T17:02:07.393610+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mental retardation, X-linked 1, 309530 (3) for gene: IQSEC2","entity_name":"IQSEC2","entity_type":"gene"},{"created":"2023-11-02T17:02:06.076908+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Nephronophthisis 2, infantile, 602088 (3) for gene: INVS","entity_name":"INVS","entity_type":"gene"},{"created":"2023-11-02T17:02:04.792811+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Joubert syndrome 1, 213300 (3) for gene: INPP5E","entity_name":"INPP5E","entity_type":"gene"},{"created":"2023-11-02T17:02:03.796603+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type, 608971 (3) for gene: IL7R","entity_name":"IL7R","entity_type":"gene"},{"created":"2023-11-02T17:02:02.573149+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Severe combined immunodeficiency, X-linked, 300400 (3) for gene: IL2RG","entity_name":"IL2RG","entity_type":"gene"},{"created":"2023-11-02T17:02:00.895020+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mental retardation, X-linked 21/34, 300143 (3) for gene: IL1RAPL1","entity_name":"IL1RAPL1","entity_type":"gene"},{"created":"2023-11-02T17:01:59.289997+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Immunodeficiency 15, 615592 (3) for gene: IKBKB","entity_name":"IKBKB","entity_type":"gene"},{"created":"2023-11-02T17:01:58.408224+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Neuronopathy, distal hereditary motor, type VI, 604320 (3) for gene: IGHMBP2","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2023-11-02T17:01:57.104329+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis Ih, 607014 (3) for gene: IDUA","entity_name":"IDUA","entity_type":"gene"},{"created":"2023-11-02T17:01:55.878966+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis II, 309900 (3) for gene: IDS","entity_name":"IDS","entity_type":"gene"},{"created":"2023-11-02T17:01:54.783845+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hydrolethalus syndrome, 236680 (3) for gene: HYLS1","entity_name":"HYLS1","entity_type":"gene"},{"created":"2023-11-02T17:01:53.486571+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mental retardation, X-linked syndromic, Turner type, 300706 (3) for gene: HUWE1","entity_name":"HUWE1","entity_type":"gene"},{"created":"2023-11-02T17:01:52.190449+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes 3-beta-hydroxysteroid dehydrogenase, type II, deficiency, 201810 (3) for gene: HSD3B2","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2023-11-02T17:01:50.820238+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes D-bifunctional protein deficiency, 261515 (3) for gene: HSD17B4","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2023-11-02T17:01:49.786541+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes HSD10 mitochondrial disease for gene: HSD17B10","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2023-11-02T17:01:48.488490+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hermansky-Pudlak syndrome 6, 614075 (3) for gene: HPS6","entity_name":"HPS6","entity_type":"gene"},{"created":"2023-11-02T17:01:47.195973+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hermansky-Pudlak syndrome 5, 614074 (3) for gene: HPS5","entity_name":"HPS5","entity_type":"gene"},{"created":"2023-11-02T17:01:45.867125+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hermansky-Pudlak syndrome 4, 614073 (3) for gene: HPS4","entity_name":"HPS4","entity_type":"gene"},{"created":"2023-11-02T17:01:44.801710+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hermansky-Pudlak syndrome 3, 614072 (3) for gene: HPS3","entity_name":"HPS3","entity_type":"gene"},{"created":"2023-11-02T17:01:43.504294+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hermansky-Pudlak syndrome 1, 203300 (3) for gene: HPS1","entity_name":"HPS1","entity_type":"gene"},{"created":"2023-11-02T17:01:42.183058+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Lesch-Nyhan syndrome, 300322 (3) for gene: HPRT1","entity_name":"HPRT1","entity_type":"gene"},{"created":"2023-11-02T17:01:41.266325+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Tyrosinemia, type III, 276710 (3) for gene: HPD","entity_name":"HPD","entity_type":"gene"},{"created":"2023-11-02T17:01:39.936512+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes HMG-CoA synthase-2 deficiency, 605911 (3) for gene: HMGCS2","entity_name":"HMGCS2","entity_type":"gene"},{"created":"2023-11-02T17:01:38.673548+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes HMG-CoA lyase deficiency, 246450 (3) for gene: HMGCL","entity_name":"HMGCL","entity_type":"gene"},{"created":"2023-11-02T17:01:37.364529+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Holocarboxylase synthetase deficiency, 253270 (3) for gene: HLCS","entity_name":"HLCS","entity_type":"gene"},{"created":"2023-11-02T17:01:36.402452+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes 3-hydroxyisobutryl-CoA hydrolase deficiency, 250620 (3) for gene: HIBCH","entity_name":"HIBCH","entity_type":"gene"},{"created":"2023-11-02T17:01:35.093910+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis type IIIC (Sanfilippo C), 252930 (3) for gene: HGSNAT","entity_name":"HGSNAT","entity_type":"gene"},{"created":"2023-11-02T17:01:33.766364+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hemochromatosis, type 2A, 602390 (3) for gene: HFE2","entity_name":"HFE2","entity_type":"gene"},{"created":"2023-11-02T17:01:32.789287+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Sandhoff disease, infantile, juvenile, and adult forms, 268800 (3) for gene: HEXB","entity_name":"HEXB","entity_type":"gene"},{"created":"2023-11-02T17:01:31.497608+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Tay-Sachs disease, 272800 (3) for gene: HEXA","entity_name":"HEXA","entity_type":"gene"},{"created":"2023-11-02T17:01:30.182503+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ), 309541 (3) for gene: HCFC1","entity_name":"HCFC1","entity_type":"gene"},{"created":"2023-11-02T17:01:28.875254+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Thalassemias, beta-, 613985 (3) for gene: HBB","entity_name":"HBB","entity_type":"gene"},{"created":"2023-11-02T17:01:27.963298+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Neutropenia, severe congenital 3, autosomal recessive, 610738 (3) for gene: HAX1","entity_name":"HAX1","entity_type":"gene"},{"created":"2023-11-02T17:01:26.673746+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hemochromatosis, type 2B, 613313 (3) for gene: HAMP","entity_name":"HAMP","entity_type":"gene"},{"created":"2023-11-02T17:01:25.363276+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Trifunctional protein deficiency, 609015 (3) for gene: HADHB","entity_name":"HADHB","entity_type":"gene"},{"created":"2023-11-02T17:01:24.368813+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fatty liver, acute, of pregnancy, 609016 (3) for gene: HADHA","entity_name":"HADHA","entity_type":"gene"},{"created":"2023-11-02T17:01:22.971733+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes 3-hydroxyacyl-CoA dehydrogenase deficiency, 231530 (3) for gene: HADH","entity_name":"HADH","entity_type":"gene"},{"created":"2023-11-02T17:01:21.680102+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis VII, 253220 (3) for gene: GUSB","entity_name":"GUSB","entity_type":"gene"},{"created":"2023-11-02T17:01:20.382481+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leber congenital amaurosis 1, 204000 (3) for gene: GUCY2D","entity_name":"GUCY2D","entity_type":"gene"},{"created":"2023-11-02T17:01:19.388906+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glutathione synthetase deficiency, 266130 (3) for gene: GSS","entity_name":"GSS","entity_type":"gene"},{"created":"2023-11-02T17:01:18.064481+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Chudley-McCullough syndrome, 604213 (3) for gene: GPSM2","entity_name":"GPSM2","entity_type":"gene"},{"created":"2023-11-02T17:01:16.705688+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ocular albinism, type I, Nettleship-Falls type, 300500 (3) for gene: GPR143","entity_name":"GPR143","entity_type":"gene"},{"created":"2023-11-02T17:01:15.463300+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Simpson-Golabi-Behmel syndrome, type 1, 312870 (3) for gene: GPC3","entity_name":"GPC3","entity_type":"gene"},{"created":"2023-11-02T17:01:14.501605+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Geroderma osteodysplasticum, 231070 (3) for gene: GORAB","entity_name":"GORAB","entity_type":"gene"},{"created":"2023-11-02T17:01:13.196686+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis type IIID, 252940 (3) for gene: GNS","entity_name":"GNS","entity_type":"gene"},{"created":"2023-11-02T17:01:11.800367+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucolipidosis III gamma, 252605 (3) for gene: GNPTG","entity_name":"GNPTG","entity_type":"gene"},{"created":"2023-11-02T17:01:10.789966+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucolipidosis III alpha/beta, 252600 (3) for gene: GNPTAB","entity_name":"GNPTAB","entity_type":"gene"},{"created":"2023-11-02T17:01:09.394619+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Chondrodysplasia punctata, rhizomelic, type 2, 222765 (3) for gene: GNPAT","entity_name":"GNPAT","entity_type":"gene"},{"created":"2023-11-02T17:01:07.985288+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Inclusion body myopathy, autosomal recessive, 600737 (3) for gene: GNE","entity_name":"GNE","entity_type":"gene"},{"created":"2023-11-02T17:01:06.571064+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Intellectual developmental disorder with cardiac arrhythmia, 617173 (3), Autosomal recessive for gene: GNB5","entity_name":"GNB5","entity_type":"gene"},{"created":"2023-11-02T17:01:05.585982+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Arthrogryposis, lethal, with anterior horn cell disease, 611890 (3) for gene: GLE1","entity_name":"GLE1","entity_type":"gene"},{"created":"2023-11-02T17:01:04.289998+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glycine encephalopathy, 605899 (3) for gene: GLDC","entity_name":"GLDC","entity_type":"gene"},{"created":"2023-11-02T17:01:03.103549+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis type IVB (Morquio), 253010 (3) for gene: GLB1","entity_name":"GLB1","entity_type":"gene"},{"created":"2023-11-02T17:01:02.095955+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fabry disease, MIM#301500 for gene: GLA","entity_name":"GLA","entity_type":"gene"},{"created":"2023-11-02T17:01:00.673217+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Charcot-Marie-Tooth neuropathy, X-linked dominant, 1\t(MIM#302800) for gene: GJB1","entity_name":"GJB1","entity_type":"gene"},{"created":"2023-11-02T17:00:59.365648+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Laron dwarfism, 262500 (3) for gene: GHR","entity_name":"GHR","entity_type":"gene"},{"created":"2023-11-02T17:00:58.096861+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Combined oxidative phosphorylation deficiency 1, 609060 (3) for gene: GFM1","entity_name":"GFM1","entity_type":"gene"},{"created":"2023-11-02T17:00:57.111550+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Chondrodysplasia, Grebe type, 200700 (3) for gene: GDF5","entity_name":"GDF5","entity_type":"gene"},{"created":"2023-11-02T17:00:55.865538+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Right atrial isomerism, 208530 (3) for gene: GDF1","entity_name":"GDF1","entity_type":"gene"},{"created":"2023-11-02T17:00:54.395755+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Charcot-Marie-Tooth disease, recessive intermediate, A, 608340 (3) for gene: GDAP1","entity_name":"GDAP1","entity_type":"gene"},{"created":"2023-11-02T17:00:53.499117+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dystonia, DOPA-responsive, with or without hyperphenylalaninemia, 128230 (3) for gene: GCH1","entity_name":"GCH1","entity_type":"gene"},{"created":"2023-11-02T17:00:52.293645+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glutaricaciduria, type I, 231670 (3) for gene: GCDH","entity_name":"GCDH","entity_type":"gene"}]}