{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=530","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=528","results":[{"created":"2023-11-02T17:00:50.973210+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glycogen storage disease IV, 232500 (3) for gene: GBE1","entity_name":"GBE1","entity_type":"gene"},{"created":"2023-11-02T17:00:49.540267+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cerebral creatine deficiency syndrome 3, 612718 (3) for gene: GATM","entity_name":"GATM","entity_type":"gene"},{"created":"2023-11-02T17:00:48.503778+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cerebral creatine deficiency syndrome 2, 612736 (3) for gene: GAMT","entity_name":"GAMT","entity_type":"gene"},{"created":"2023-11-02T17:00:47.163276+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Galactosemia, 230400 (3) for gene: GALT","entity_name":"GALT","entity_type":"gene"},{"created":"2023-11-02T17:00:45.921333+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis IVA, 253000 (3) for gene: GALNS","entity_name":"GALNS","entity_type":"gene"},{"created":"2023-11-02T17:00:44.573528+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Krabbe disease, 245200 (3) for gene: GALC","entity_name":"GALC","entity_type":"gene"},{"created":"2023-11-02T17:00:43.590788+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glycogen storage disease II, 232300 (3) for gene: GAA","entity_name":"GAA","entity_type":"gene"},{"created":"2023-11-02T17:00:42.187035+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dursun syndrome, 612541 (3) for gene: G6PC3","entity_name":"G6PC3","entity_type":"gene"},{"created":"2023-11-02T17:00:40.806641+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glycogen storage disease Ia, 232200 (3) for gene: G6PC","entity_name":"G6PC","entity_type":"gene"},{"created":"2023-11-02T17:00:39.963345+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fucosidosis, 230000 (3) for gene: FUCA1","entity_name":"FUCA1","entity_type":"gene"},{"created":"2023-11-02T17:00:38.503973+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 9, 309549 (3) for gene: FTSJ1","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2023-11-02T17:00:37.184475+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fraser syndrome, 219000 (3) for gene: FREM2","entity_name":"FREM2","entity_type":"gene"},{"created":"2023-11-02T17:00:35.790187+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fraser syndrome, 219000 (3) for gene: FRAS1","entity_name":"FRAS1","entity_type":"gene"},{"created":"2023-11-02T17:00:34.796411+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mitochondrial complex I deficiency, 252010 (3) for gene: FOXRED1","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2023-11-02T17:00:33.470303+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes T-cell immunodeficiency, congenital alopecia, and nail dystrophy, 601705 (3) for gene: FOXN1","entity_name":"FOXN1","entity_type":"gene"},{"created":"2023-11-02T17:00:32.174310+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fragile X syndrome for gene: FMR1","entity_name":"FMR1","entity_type":"gene"},{"created":"2023-11-02T17:00:31.227462+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes FG syndrome 2, 300321 (3) for gene: FLNA","entity_name":"FLNA","entity_type":"gene"},{"created":"2023-11-02T17:00:29.888294+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, 4, 253800 (3) for gene: FKTN","entity_name":"FKTN","entity_type":"gene"},{"created":"2023-11-02T17:00:28.566116+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, 5, 613153 (3) for gene: FKRP","entity_name":"FKRP","entity_type":"gene"},{"created":"2023-11-02T17:00:27.172073+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Bruck syndrome 1, 259450 (3) for gene: FKBP10","entity_name":"FKBP10","entity_type":"gene"},{"created":"2023-11-02T17:00:26.276749+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Emery-Dreifuss muscular dystrophy 6, X-linked, 300696 (3) for gene: FHL1","entity_name":"FHL1","entity_type":"gene"},{"created":"2023-11-02T17:00:24.896233+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fumarase deficiency, 606812 (3) for gene: FH","entity_name":"FH","entity_type":"gene"},{"created":"2023-11-02T17:00:23.596427+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Parkinson disease 15, autosomal recessive, 260300 (3) for gene: FBXO7","entity_name":"FBXO7","entity_type":"gene"},{"created":"2023-11-02T17:00:22.689671+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fructose-1,6-bisphosphatase deficiency, 229700 (3) for gene: FBP1","entity_name":"FBP1","entity_type":"gene"},{"created":"2023-11-02T17:00:21.264518+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hennekam lymphangiectasia-lymphedema syndrome 2, 616006 (3) for gene: FAT4","entity_name":"FAT4","entity_type":"gene"},{"created":"2023-11-02T17:00:19.794927+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group L, 614083 (3) for gene: FANCL","entity_name":"FANCL","entity_type":"gene"},{"created":"2023-11-02T17:00:18.518044+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group I, 609053 (3) for gene: FANCI","entity_name":"FANCI","entity_type":"gene"},{"created":"2023-11-02T17:00:17.485932+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group G, 614082 (3) for gene: FANCG","entity_name":"FANCG","entity_type":"gene"},{"created":"2023-11-02T17:00:16.196069+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group F, 603467 (3) for gene: FANCF","entity_name":"FANCF","entity_type":"gene"},{"created":"2023-11-02T17:00:14.975102+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group E, 600901 (3) for gene: FANCE","entity_name":"FANCE","entity_type":"gene"},{"created":"2023-11-02T17:00:13.664491+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group D2, 227646 (3) for gene: FANCD2","entity_name":"FANCD2","entity_type":"gene"},{"created":"2023-11-02T17:00:12.782335+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group C, 227645 (3) for gene: FANCC","entity_name":"FANCC","entity_type":"gene"},{"created":"2023-11-02T17:00:11.031089+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group B, 300514 (3) for gene: FANCB","entity_name":"FANCB","entity_type":"gene"},{"created":"2023-11-02T17:00:09.603553+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group A, 227650 (3) for gene: FANCA","entity_name":"FANCA","entity_type":"gene"},{"created":"2023-11-02T17:00:08.046340+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leukodystrophy, hypomyelinating, 5, 610532 (3) for gene: FAM126A","entity_name":"FAM126A","entity_type":"gene"},{"created":"2023-11-02T17:00:05.132318+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 I, 276700 (3) for gene: FAH","entity_name":"FAH","entity_type":"gene"},{"created":"2023-11-02T17:00:01.401532+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dysprothrombinaemia, 613679; Hypoprothrombinaemia (MIM#613679) for gene: F2","entity_name":"F2","entity_type":"gene"},{"created":"2023-11-02T16:59:59.667390+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pontocerebellar hypoplasia, type 1C, 616081 (3) for gene: EXOSC8","entity_name":"EXOSC8","entity_type":"gene"},{"created":"2023-11-02T16:59:58.694344+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pontocerebellar hypoplasia, type 1B, 614678 (3) for gene: EXOSC3","entity_name":"EXOSC3","entity_type":"gene"},{"created":"2023-11-02T16:59:57.381656+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ellis-van Creveld syndrome, 225500 (3) for gene: EVC2","entity_name":"EVC2","entity_type":"gene"},{"created":"2023-11-02T16:59:56.100977+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ellis-van Creveld syndrome, 225500 (3) for gene: EVC","entity_name":"EVC","entity_type":"gene"},{"created":"2023-11-02T16:59:55.188466+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ethylmalonic encephalopathy, 602473 (3) for gene: ETHE1","entity_name":"ETHE1","entity_type":"gene"},{"created":"2023-11-02T16:59:53.898398+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glutaric acidemia IIC, 231680 (3) for gene: ETFDH","entity_name":"ETFDH","entity_type":"gene"},{"created":"2023-11-02T16:59:52.633395+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glutaric acidemia IIB, 231680 (3) for gene: ETFB","entity_name":"ETFB","entity_type":"gene"},{"created":"2023-11-02T16:59:51.292064+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glutaric acidemia IIA, 231680 (3) for gene: ETFA","entity_name":"ETFA","entity_type":"gene"},{"created":"2023-11-02T16:59:50.377150+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes SC phocomelia syndrome, 269000 (3) for gene: ESCO2","entity_name":"ESCO2","entity_type":"gene"},{"created":"2023-11-02T16:59:48.898289+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cockayne syndrome, type A, 216400 (3) for gene: ERCC8","entity_name":"ERCC8","entity_type":"gene"},{"created":"2023-11-02T16:59:47.672619+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cockayne syndrome, type B, 133540 (3) for gene: ERCC6","entity_name":"ERCC6","entity_type":"gene"},{"created":"2023-11-02T16:59:46.588372+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Xeroderma pigmentosum, group G, 278780 (3) for gene: ERCC5","entity_name":"ERCC5","entity_type":"gene"},{"created":"2023-11-02T16:59:45.292753+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group Q, 615272 (3) for gene: ERCC4","entity_name":"ERCC4","entity_type":"gene"},{"created":"2023-11-02T16:59:43.969277+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cerebrooculofacioskeletal syndrome 2, 610756 (3) for gene: ERCC2","entity_name":"ERCC2","entity_type":"gene"},{"created":"2023-11-02T16:59:42.574317+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Vici syndrome, 242840 (3) for gene: EPG5","entity_name":"EPG5","entity_type":"gene"},{"created":"2023-11-02T16:59:41.498281+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hypophosphatemic rickets, autosomal recessive, 2, 613312 (3) for gene: ENPP1","entity_name":"ENPP1","entity_type":"gene"},{"created":"2023-11-02T16:59:40.382318+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Emery-Dreifuss muscular dystrophy 1, X-linked, 310300 (3) for gene: EMD","entity_name":"EMD","entity_type":"gene"},{"created":"2023-11-02T16:59:39.164405+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dysautonomia, familial, 223900 (3) for gene: ELP1","entity_name":"ELP1","entity_type":"gene"},{"created":"2023-11-02T16:59:37.887071+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leukoencephalopathy with vanishing white matter, 603896 (3) for gene: EIF2B5","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2023-11-02T16:59:36.871756+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leukoencephaly with vanishing white matter, 603896 (3) for gene: EIF2B4","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2023-11-02T16:59:35.394560+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leukoencephalopathy with vanishing white matter, 603896 (3) for gene: EIF2B3","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2023-11-02T16:59:34.205564+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leukoencephalopathy with vanishing white matter, 603896 (3) for gene: EIF2B2","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2023-11-02T16:59:33.282360+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leukoencephalopathy with vanishing white matter, 603896 (3) for gene: EIF2B1","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2023-11-02T16:59:32.063487+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Wolcott-Rallison syndrome, 226980 (3) for gene: EIF2AK3","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2023-11-02T16:59:30.610115+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ectodermal dysplasia 1, hypohidrotic, X-linked, 305100 (3) for gene: EDA","entity_name":"EDA","entity_type":"gene"},{"created":"2023-11-02T16:59:29.288660+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, 616277 (3) for gene: ECHS1","entity_name":"ECHS1","entity_type":"gene"},{"created":"2023-11-02T16:59:28.404399+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, limb-girdle, type 2B, 253601 (3) for gene: DYSF","entity_name":"DYSF","entity_type":"gene"},{"created":"2023-11-02T16:59:27.165497+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Short-rib thoracic dysplasia 3 with or without polydactyly, 613091 (3) for gene: DYNC2H1","entity_name":"DYNC2H1","entity_type":"gene"},{"created":"2023-11-02T16:59:25.688697+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dyggve-Melchior-Clausen disease, 223800 (3) for gene: DYM","entity_name":"DYM","entity_type":"gene"},{"created":"2023-11-02T16:59:24.695920+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Myasthenic syndrome, congenital, 10, 254300 (3) for gene: DOK7","entity_name":"DOK7","entity_type":"gene"},{"created":"2023-11-02T16:59:23.496621+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Adams-Oliver syndrome 2, 614219 (3) for gene: DOCK6","entity_name":"DOCK6","entity_type":"gene"},{"created":"2023-11-02T16:59:22.186902+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Immunodeficiency-centromeric instability-facial anomalies syndrome 1, 242860 (3) for gene: DNMT3B","entity_name":"DNMT3B","entity_type":"gene"},{"created":"2023-11-02T16:59:20.878816+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ciliary dyskinesia, primary, 9, with or without situs inversus, 612444 (3) for gene: DNAI2","entity_name":"DNAI2","entity_type":"gene"},{"created":"2023-11-02T16:59:19.806070+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ciliary dyskinesia, primary, 1, with or without situs inversus, 244400 (3) for gene: DNAI1","entity_name":"DNAI1","entity_type":"gene"},{"created":"2023-11-02T16:59:18.477538+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ciliary dyskinesia, primary, 3, with or without situs inversus, 608644 (3) for gene: DNAH5","entity_name":"DNAH5","entity_type":"gene"},{"created":"2023-11-02T16:59:17.190225+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 (3) for gene: DNAH11","entity_name":"DNAH11","entity_type":"gene"},{"created":"2023-11-02T16:59:16.282047+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Duchenne muscular dystrophy, 310200 (3) for gene: DMD","entity_name":"DMD","entity_type":"gene"},{"created":"2023-11-02T16:59:14.998600+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Spondylocostal dysostosis 1, autosomal recessive, 277300 (3) for gene: DLL3","entity_name":"DLL3","entity_type":"gene"},{"created":"2023-11-02T16:59:13.785924+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 90, 300850 (3) for gene: DLG3","entity_name":"DLG3","entity_type":"gene"},{"created":"2023-11-02T16:59:12.477246+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dihydrolipoamide dehydrogenase deficiency, 246900 (3) for gene: DLD","entity_name":"DLD","entity_type":"gene"},{"created":"2023-11-02T16:59:11.478614+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dyskeratosis congenita, X-linked, 305000 (3) for gene: DKC1","entity_name":"DKC1","entity_type":"gene"},{"created":"2023-11-02T16:59:10.189785+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Perlman syndrome, 267000 (3) for gene: DIS3L2","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2023-11-02T16:59:08.869787+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Retinitis pigmentosa 59, 613861 (3) for gene: DHDDS","entity_name":"DHDDS","entity_type":"gene"},{"created":"2023-11-02T16:59:07.591213+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Smith-Lemli-Opitz syndrome, 270400 (3) for gene: DHCR7","entity_name":"DHCR7","entity_type":"gene"},{"created":"2023-11-02T16:59:06.503617+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Desmosterolosis, 602398 (3) for gene: DHCR24","entity_name":"DHCR24","entity_type":"gene"},{"created":"2023-11-02T16:59:05.182632+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), 251880 (3) for gene: DGUOK","entity_name":"DGUOK","entity_type":"gene"},{"created":"2023-11-02T16:59:03.888988+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes ?Diarrhea 7, protein-losing enteropathy type for gene: DGAT1","entity_name":"DGAT1","entity_type":"gene"},{"created":"2023-11-02T16:59:02.878837+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Warsaw breakage syndrome, 613398 (3) for gene: DDX11","entity_name":"DDX11","entity_type":"gene"},{"created":"2023-11-02T16:59:01.402421+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Aromatic L-amino acid decarboxylase deficiency, 608643 (3) for gene: DDC","entity_name":"DDC","entity_type":"gene"},{"created":"2023-11-02T16:58:59.969118+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Lissencephaly, X-linked, 300067 (3) for gene: DCX","entity_name":"DCX","entity_type":"gene"},{"created":"2023-11-02T16:58:58.689620+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, Athabascan type, 602450 (3) for gene: DCLRE1C","entity_name":"DCLRE1C","entity_type":"gene"},{"created":"2023-11-02T16:58:57.768638+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Woodhouse-Sakati syndrome, 241080 (3) for gene: DCAF17","entity_name":"DCAF17","entity_type":"gene"},{"created":"2023-11-02T16:58:56.443737+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Maple syrup urine disease, type II, 248600 (3) for gene: DBT","entity_name":"DBT","entity_type":"gene"},{"created":"2023-11-02T16:58:55.072663+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes D-2-hydroxyglutaric aciduria, 600721 (3) for gene: D2HGDH","entity_name":"D2HGDH","entity_type":"gene"},{"created":"2023-11-02T16:58:54.088055+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Bile acid synthesis defect, congenital, 3, 613812 (3) for gene: CYP7B1","entity_name":"CYP7B1","entity_type":"gene"},{"created":"2023-11-02T16:58:52.773380+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cerebrotendinous xanthomatosis, 213700 (3) for gene: CYP27A1","entity_name":"CYP27A1","entity_type":"gene"},{"created":"2023-11-02T16:58:51.581423+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300 (3) for gene: CYP1B1","entity_name":"CYP1B1","entity_type":"gene"},{"created":"2023-11-02T16:58:50.175574+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes 17,20-lyase deficiency, isolated, 202110 (3) for gene: CYP17A1","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2023-11-02T16:58:49.099699+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hypoaldosteronism, congenital, due to CMO I deficiency, 203400 (3) for gene: CYP11B2","entity_name":"CYP11B2","entity_type":"gene"},{"created":"2023-11-02T16:58:47.801859+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, 613743 (3) for gene: CYP11A1","entity_name":"CYP11A1","entity_type":"gene"},{"created":"2023-11-02T16:58:46.572283+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Chronic granulomatous disease, X-linked, 306400 (3) for gene: CYBB","entity_name":"CYBB","entity_type":"gene"},{"created":"2023-11-02T16:58:45.672805+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Chronic granulomatous disease, autosomal, due to deficiency of CYBA, 233690 (3) for gene: CYBA","entity_name":"CYBA","entity_type":"gene"},{"created":"2023-11-02T16:58:44.378494+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 15 (Cabezas type), 300354 (3) for gene: CUL4B","entity_name":"CUL4B","entity_type":"gene"}]}