{"count":221284,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1647","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1645","results":[{"created":"2020-08-27T21:00:01.628181+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Xeroderma pigmentosum for gene: DDB2","entity_name":"DDB2","entity_type":"gene"},{"created":"2020-08-27T21:00:01.330815+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Lissencephaly, X-linked for gene: DCX","entity_name":"DCX","entity_type":"gene"},{"created":"2020-08-27T21:00:01.035195+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Severe combined immunodeficiency, Athabascan type for gene: DCLRE1C","entity_name":"DCLRE1C","entity_type":"gene"},{"created":"2020-08-27T21:00:00.736648+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Maple syrup urine disease for gene: DBT","entity_name":"DBT","entity_type":"gene"},{"created":"2020-08-27T21:00:00.433354+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes D-2-hydroxyglutaric aciduria for gene: D2HGDH","entity_name":"D2HGDH","entity_type":"gene"},{"created":"2020-08-27T21:00:00.174097+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ichthyosis, congenital, autosomal recessive for gene: CYP4F22","entity_name":"CYP4F22","entity_type":"gene"},{"created":"2020-08-27T20:59:59.745490+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Vitamin D-dependent rickets, type I for gene: CYP27B1","entity_name":"CYP27B1","entity_type":"gene"},{"created":"2020-08-27T20:59:59.229675+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cerebrotendinous xanthomatosis for gene: CYP27A1","entity_name":"CYP27A1","entity_type":"gene"},{"created":"2020-08-27T20:59:58.932676+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency for gene: CYP21A2","entity_name":"CYP21A2","entity_type":"gene"},{"created":"2020-08-27T20:59:58.637829+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency for gene: CYP11B1","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2020-08-27T20:59:58.339955+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete for gene: CYP11A1","entity_name":"CYP11A1","entity_type":"gene"},{"created":"2020-08-27T20:59:58.041145+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Chronic granulomatous disease for gene: CYBB","entity_name":"CYBB","entity_type":"gene"},{"created":"2020-08-27T20:59:57.739359+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Chronic granulomatous disease for gene: CYBA","entity_name":"CYBA","entity_type":"gene"},{"created":"2020-08-27T20:59:57.442986+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes 3-M syndrome for gene: CUL7","entity_name":"CUL7","entity_type":"gene"},{"created":"2020-08-27T20:59:57.142794+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Megaloblastic anemia-1, Finnish type for gene: CUBN","entity_name":"CUBN","entity_type":"gene"},{"created":"2020-08-27T20:59:56.845824+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Pycnodysostosis for gene: CTSK","entity_name":"CTSK","entity_type":"gene"},{"created":"2020-08-27T20:59:56.546776+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ceroid lipofuscinosis, neuronal, 10 for gene: CTSD","entity_name":"CTSD","entity_type":"gene"},{"created":"2020-08-27T20:59:56.042864+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cystinosis for gene: CTNS","entity_name":"CTNS","entity_type":"gene"},{"created":"2020-08-27T20:59:55.741356+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Coats plus syndrome for gene: CTC1","entity_name":"CTC1","entity_type":"gene"},{"created":"2020-08-27T20:59:55.444835+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Epilepsy, progressive myoclonic 1A for gene: CSTB","entity_name":"CSTB","entity_type":"gene"},{"created":"2020-08-27T20:59:55.142079+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Pulmonary alveolar proteinosis for gene: CSF2RA","entity_name":"CSF2RA","entity_type":"gene"},{"created":"2020-08-27T20:59:54.846367+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Myofibrillar myopathy for gene: CRYAB","entity_name":"CRYAB","entity_type":"gene"},{"created":"2020-08-27T20:59:54.550558+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Osteogenesis imperfecta, type VII for gene: CRTAP","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-08-27T20:59:54.318821+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Crisponi syndrome for gene: CRLF1","entity_name":"CRLF1","entity_type":"gene"},{"created":"2020-08-27T20:59:54.026158+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Rubinstein-Taybi syndrome for gene: CREBBP","entity_name":"CREBBP","entity_type":"gene"},{"created":"2020-08-27T20:59:53.437562+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Carnitine palmitoyltransferase 2 deficiency for gene: CPT2","entity_name":"CPT2","entity_type":"gene"},{"created":"2020-08-27T20:59:53.141888+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Carnitine palmitoyltransferase I deficiency for gene: CPT1A","entity_name":"CPT1A","entity_type":"gene"},{"created":"2020-08-27T20:59:52.848284+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Carbamoylphosphate synthetase I deficiency for gene: CPS1","entity_name":"CPS1","entity_type":"gene"},{"created":"2020-08-27T20:59:52.546382+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital myasthenic syndrome for gene: COLQ","entity_name":"COLQ","entity_type":"gene"},{"created":"2020-08-27T20:59:52.251417+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa dystrophica for gene: COL7A1","entity_name":"COL7A1","entity_type":"gene"},{"created":"2020-08-27T20:59:52.017439+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ullrich congenital muscular dystrophy for gene: COL6A3","entity_name":"COL6A3","entity_type":"gene"},{"created":"2020-08-27T20:59:51.720585+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ullrich congenital muscular dystrophy for gene: COL6A2","entity_name":"COL6A2","entity_type":"gene"},{"created":"2020-08-27T20:59:51.420648+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ullrich congenital muscular dystrophy for gene: COL6A1","entity_name":"COL6A1","entity_type":"gene"},{"created":"2020-08-27T20:59:50.839528+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ehlers-Danlos syndrome for gene: COL5A2","entity_name":"COL5A2","entity_type":"gene"},{"created":"2020-08-27T20:59:50.544197+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ehlers-Danlos syndrome, type I for gene: COL5A1","entity_name":"COL5A1","entity_type":"gene"},{"created":"2020-08-27T20:59:50.246798+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Alport syndrome for gene: COL4A5","entity_name":"COL4A5","entity_type":"gene"},{"created":"2020-08-27T20:59:49.950251+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Alport syndrome for gene: COL4A4","entity_name":"COL4A4","entity_type":"gene"},{"created":"2020-08-27T20:59:49.656886+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Alport syndrome for gene: COL4A3","entity_name":"COL4A3","entity_type":"gene"},{"created":"2020-08-27T20:59:49.418848+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ehlers-Danlos syndrome, type IV for gene: COL3A1","entity_name":"COL3A1","entity_type":"gene"},{"created":"2020-08-27T20:59:49.121763+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Stickler syndrome for gene: COL2A1","entity_name":"COL2A1","entity_type":"gene"},{"created":"2020-08-27T20:59:48.826123+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Osteogenesis imperfecta, type II for gene: COL1A2","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-08-27T20:59:48.531981+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Osteogenesis imperfecta, type I for gene: COL1A1","entity_name":"COL1A1","entity_type":"gene"},{"created":"2020-08-27T20:59:48.235521+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa, junctional, non-Herlitz type for gene: COL17A1","entity_name":"COL17A1","entity_type":"gene"},{"created":"2020-08-27T20:59:47.723024+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Otospondylomegaepiphyseal dysplasia for gene: COL11A2","entity_name":"COL11A2","entity_type":"gene"},{"created":"2020-08-27T20:59:47.431296+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Stickler syndrome for gene: COL11A1","entity_name":"COL11A1","entity_type":"gene"},{"created":"2020-08-27T20:59:47.134827+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Deafness, non-syndromic, autosomal dominant for gene: COCH","entity_name":"COCH","entity_type":"gene"},{"created":"2020-08-27T20:59:46.842069+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Achromatopsia-3 for gene: CNGB3","entity_name":"CNGB3","entity_type":"gene"},{"created":"2020-08-27T20:59:46.542097+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Usher syndrome, type 3A for gene: CLRN1","entity_name":"CLRN1","entity_type":"gene"},{"created":"2020-08-27T20:59:46.247861+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ceroid lipofuscinosis, neuronal, 8 for gene: CLN8","entity_name":"CLN8","entity_type":"gene"},{"created":"2020-08-27T20:59:45.956785+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ceroid lipofuscinosis, neuronal, 6 for gene: CLN6","entity_name":"CLN6","entity_type":"gene"},{"created":"2020-08-27T20:59:45.658229+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ceroid lipofuscinosis, neuronal, 5 for gene: CLN5","entity_name":"CLN5","entity_type":"gene"},{"created":"2020-08-27T20:59:45.423445+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ceroid lipofuscinosis, neuronal, 3 for gene: CLN3","entity_name":"CLN3","entity_type":"gene"},{"created":"2020-08-27T20:59:45.125842+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hypomagnesemia 5, renal, with ocular involvement for gene: CLDN19","entity_name":"CLDN19","entity_type":"gene"},{"created":"2020-08-27T20:59:44.547002+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hearing loss, non-syndromic, autosomal recessive for gene: CLDN14","entity_name":"CLDN14","entity_type":"gene"},{"created":"2020-08-27T20:59:44.247797+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Dent disease for gene: CLCN5","entity_name":"CLCN5","entity_type":"gene"},{"created":"2020-08-27T20:59:43.955772+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Pterygium syndrome for gene: CHRNG","entity_name":"CHRNG","entity_type":"gene"},{"created":"2020-08-27T20:59:43.647221+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital myasthenic syndrome for gene: CHRNE","entity_name":"CHRNE","entity_type":"gene"},{"created":"2020-08-27T20:59:43.356424+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital myasthenic syndrome for gene: CHRND","entity_name":"CHRND","entity_type":"gene"},{"created":"2020-08-27T20:59:43.120819+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital myasthenic syndrome for gene: CHRNA1","entity_name":"CHRNA1","entity_type":"gene"},{"created":"2020-08-27T20:59:42.825002+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Choroideremia for gene: CHM","entity_name":"CHM","entity_type":"gene"},{"created":"2020-08-27T20:59:42.529312+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Muscular dystrophy, congenital, megaconial type for gene: CHKB","entity_name":"CHKB","entity_type":"gene"},{"created":"2020-08-27T20:59:41.955893+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes CHARGE syndrome for gene: CHD7","entity_name":"CHD7","entity_type":"gene"},{"created":"2020-08-27T20:59:41.722609+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Developmental delay, intellectual disability, epilepsy for gene: CHD2","entity_name":"CHD2","entity_type":"gene"},{"created":"2020-08-27T20:59:41.427497+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital myasthenic syndrome for gene: CHAT","entity_name":"CHAT","entity_type":"gene"},{"created":"2020-08-27T20:59:41.131276+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cystic fibrosis for gene: CFTR","entity_name":"CFTR","entity_type":"gene"},{"created":"2020-08-27T20:59:40.831444+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Properdin deficiency, X-linked for gene: CFP","entity_name":"CFP","entity_type":"gene"},{"created":"2020-08-27T20:59:40.534308+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Nemaline myopathy for gene: CFL2","entity_name":"CFL2","entity_type":"gene"},{"created":"2020-08-27T20:59:40.234969+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital heart defects for gene: CFC1","entity_name":"CFC1","entity_type":"gene"},{"created":"2020-08-27T20:59:39.937698+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Joubert syndrome for gene: CEP290","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-08-27T20:59:39.434404+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Seckel syndrome for gene: CEP152","entity_name":"CEP152","entity_type":"gene"},{"created":"2020-08-27T20:59:39.136233+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hypotrichosis for gene: CDSN","entity_name":"CDSN","entity_type":"gene"},{"created":"2020-08-27T20:59:38.842383+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Beckwith-Wiedemann syndrome for gene: CDKN1C","entity_name":"CDKN1C","entity_type":"gene"},{"created":"2020-08-27T20:59:38.544605+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Epileptic encephalopathy, early infantile, 2 for gene: CDKL5","entity_name":"CDKL5","entity_type":"gene"},{"created":"2020-08-27T20:59:38.252850+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Usher syndrome, type 1D for gene: CDH23","entity_name":"CDH23","entity_type":"gene"},{"created":"2020-08-27T20:59:38.018894+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Deafness, autosomal recessive for gene: CDH23","entity_name":"CDH23","entity_type":"gene"},{"created":"2020-08-27T20:59:37.725697+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Anemia, congenital dyserythropoietic, type I for gene: CDAN1","entity_name":"CDAN1","entity_type":"gene"},{"created":"2020-08-27T20:59:37.432416+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Immunodeficiency, X-linked, with hyper-IgM for gene: CD40LG","entity_name":"CD40LG","entity_type":"gene"},{"created":"2020-08-27T20:59:37.135499+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Primary ciliary dyskinesia for gene: CCDC40","entity_name":"CCDC40","entity_type":"gene"},{"created":"2020-08-27T20:59:36.841476+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Primary ciliary dyskinesia for gene: CCDC39","entity_name":"CCDC39","entity_type":"gene"},{"created":"2020-08-27T20:59:36.331056+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Joubert syndrome for gene: CC2D2A","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2020-08-27T20:59:36.041384+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Homocystinuria, B6-responsive and nonresponsive types for gene: CBS","entity_name":"CBS","entity_type":"gene"},{"created":"2020-08-27T20:59:35.735188+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia for gene: CBL","entity_name":"CBL","entity_type":"gene"},{"created":"2020-08-27T20:59:35.437250+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Caveolinopathy for gene: CAV3","entity_name":"CAV3","entity_type":"gene"},{"created":"2020-08-27T20:59:35.141452+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb-girdle, type IC, for gene: CAV3","entity_name":"CAV3","entity_type":"gene"},{"created":"2020-08-27T20:59:34.846630+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ventricular tachycardia, catecholaminergic polymorphic for gene: CASQ2","entity_name":"CASQ2","entity_type":"gene"},{"created":"2020-08-27T20:59:34.553591+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Mental retardation and microcephaly with pontine and cerebellar hypoplasia for gene: CASK","entity_name":"CASK","entity_type":"gene"},{"created":"2020-08-27T20:59:34.318771+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb-girdle, type 2A for gene: CAPN3","entity_name":"CAPN3","entity_type":"gene"},{"created":"2020-08-27T20:59:34.025573+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Night blindness, congenital stationary (complete), 1A, X-linked for gene: CACNA1F","entity_name":"CACNA1F","entity_type":"gene"},{"created":"2020-08-27T20:59:33.728202+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Episodic ataxia, type 2 for gene: CACNA1A","entity_name":"CACNA1A","entity_type":"gene"},{"created":"2020-08-27T20:59:33.144849+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Osteopetrosis, autosomal recessive 3, with renal tubular acidosis for gene: CA2","entity_name":"CA2","entity_type":"gene"},{"created":"2020-08-27T20:59:32.850050+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Spinocerebellar ataxia infantile-onset for gene: TWNK","entity_name":"TWNK","entity_type":"gene"},{"created":"2020-08-27T20:59:32.617419+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Agammaglobulinemia, X-linked 1 for gene: BTK","entity_name":"BTK","entity_type":"gene"},{"created":"2020-08-27T20:59:32.321923+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Biotinidase deficiency for gene: BTD","entity_name":"BTD","entity_type":"gene"},{"created":"2020-08-27T20:59:32.030348+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bartter syndrome with sensorineural deafness for gene: BSND","entity_name":"BSND","entity_type":"gene"},{"created":"2020-08-27T20:59:31.731367+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Berardinelli-Seip lipodystrophy for gene: BSCL2","entity_name":"BSCL2","entity_type":"gene"},{"created":"2020-08-27T20:59:31.433825+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fanconi anemia, complementation group D1 for gene: BRCA2","entity_name":"BRCA2","entity_type":"gene"},{"created":"2020-08-27T20:59:31.140959+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cardiofaciocutaneous syndrome for gene: BRAF","entity_name":"BRAF","entity_type":"gene"},{"created":"2020-08-27T20:59:30.623318+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Juvenile polyposis syndrome for gene: BMPR1A","entity_name":"BMPR1A","entity_type":"gene"},{"created":"2020-08-27T20:59:30.332358+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bloom syndrome for gene: BLM","entity_name":"BLM","entity_type":"gene"},{"created":"2020-08-27T20:59:30.047719+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Myopathy, centronuclear, autosomal recessive for gene: BIN1","entity_name":"BIN1","entity_type":"gene"}]}