{"count":221284,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1648","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1646","results":[{"created":"2020-08-27T20:59:29.731353+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 spinal muscular atrophy for gene: BICD2","entity_name":"BICD2","entity_type":"gene"},{"created":"2020-08-27T20:59:29.431449+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Complex 3 deficiency for gene: BCS1L","entity_name":"BCS1L","entity_type":"gene"},{"created":"2020-08-27T20:59:29.132052+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: BCKDHB","entity_name":"BCKDHB","entity_type":"gene"},{"created":"2020-08-27T20:59:28.831194+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: BCKDHA","entity_name":"BCKDHA","entity_type":"gene"},{"created":"2020-08-27T20:59:28.535661+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS9","entity_name":"BBS9","entity_type":"gene"},{"created":"2020-08-27T20:59:28.237583+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS7","entity_name":"BBS7","entity_type":"gene"},{"created":"2020-08-27T20:59:27.729590+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS5","entity_name":"BBS5","entity_type":"gene"},{"created":"2020-08-27T20:59:27.431519+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS4","entity_name":"BBS4","entity_type":"gene"},{"created":"2020-08-27T20:59:27.137436+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS2","entity_name":"BBS2","entity_type":"gene"},{"created":"2020-08-27T20:59:26.836767+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS12","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-08-27T20:59:26.539577+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS10","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-08-27T20:59:26.242338+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome for gene: BBS1","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-08-27T20:59:25.941517+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bile acid amidation defect for gene: BAAT","entity_name":"BAAT","entity_type":"gene"},{"created":"2020-08-27T20:59:25.644243+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Peters-Plus syndrome for gene: B3GLCT","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2020-08-27T20:59:25.345434+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Diabetes insipidus, nephrogenic for gene: AVPR2","entity_name":"AVPR2","entity_type":"gene"},{"created":"2020-08-27T20:59:24.823222+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-methylglutaconic aciduria, type I for gene: AUH","entity_name":"AUH","entity_type":"gene"},{"created":"2020-08-27T20:59:24.527720+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Alpha-thalassemia/mental retardation syndrome for gene: ATRX","entity_name":"ATRX","entity_type":"gene"},{"created":"2020-08-27T20:59:24.234948+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cholestasis, progressive familial intrahepatic 1 for gene: ATP8B1","entity_name":"ATP8B1","entity_type":"gene"},{"created":"2020-08-27T20:59:23.934216+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Wilson disease for gene: ATP7B","entity_name":"ATP7B","entity_type":"gene"},{"created":"2020-08-27T20:59:23.634620+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Occipital horn syndrome for gene: ATP7A","entity_name":"ATP7A","entity_type":"gene"},{"created":"2020-08-27T20:59:23.336879+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Menkes syndrome for gene: ATP7A","entity_name":"ATP7A","entity_type":"gene"},{"created":"2020-08-27T20:59:23.045231+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Renal tubular acidosis & hearing loss for gene: ATP6V1B1","entity_name":"ATP6V1B1","entity_type":"gene"},{"created":"2020-08-27T20:59:22.747563+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cutis laxa, autosomal recessive, type IIA for gene: ATP6V0A2","entity_name":"ATP6V0A2","entity_type":"gene"},{"created":"2020-08-27T20:59:22.445830+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Brody myopathy for gene: ATP2A1","entity_name":"ATP2A1","entity_type":"gene"},{"created":"2020-08-27T20:59:22.147703+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hemiplegic migraine for gene: ATP1A2","entity_name":"ATP1A2","entity_type":"gene"},{"created":"2020-08-27T20:59:21.639202+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ataxia-telangiectasia for gene: ATM","entity_name":"ATM","entity_type":"gene"},{"created":"2020-08-27T20:59:21.349813+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Citrullinemia for gene: ASS1","entity_name":"ASS1","entity_type":"gene"},{"created":"2020-08-27T20:59:21.048603+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Canavan disease for gene: ASPA","entity_name":"ASPA","entity_type":"gene"},{"created":"2020-08-27T20:59:20.749454+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Argininosuccinic aciduria for gene: ASL","entity_name":"ASL","entity_type":"gene"},{"created":"2020-08-27T20:59:20.454324+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 2 for gene: ARX","entity_name":"ARX","entity_type":"gene"},{"created":"2020-08-27T20:59:20.223919+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Mucopolysaccharidosis type VI (Maroteaux-Lamy) for gene: ARSB","entity_name":"ARSB","entity_type":"gene"},{"created":"2020-08-27T20:59:19.928798+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Metachromatic leukodystrophy for gene: ARSA","entity_name":"ARSA","entity_type":"gene"},{"created":"2020-08-27T20:59:19.631631+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: ARMC4","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-08-27T20:59:19.118796+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Coffin-Siris syndrome for gene: ARID1B","entity_name":"ARID1B","entity_type":"gene"},{"created":"2020-08-27T20:59:18.824465+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Arginase deficiency for gene: ARG1","entity_name":"ARG1","entity_type":"gene"},{"created":"2020-08-27T20:59:18.529349+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Periventricular heterotopia with microcephaly for gene: ARFGEF2","entity_name":"ARFGEF2","entity_type":"gene"},{"created":"2020-08-27T20:59:18.235024+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Androgen insensitivity for gene: AR","entity_name":"AR","entity_type":"gene"},{"created":"2020-08-27T20:59:17.936450+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia for gene: APTX","entity_name":"APTX","entity_type":"gene"},{"created":"2020-08-27T20:59:17.638578+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Apolipoprotein B deficiency for gene: APOB","entity_name":"APOB","entity_type":"gene"},{"created":"2020-08-27T20:59:17.346080+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Adenomatous polyposis coli, attenuated for gene: APC","entity_name":"APC","entity_type":"gene"},{"created":"2020-08-27T20:59:17.048297+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Adenomatous polyposis coli for gene: APC","entity_name":"APC","entity_type":"gene"},{"created":"2020-08-27T20:59:16.750444+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hermansky-Pudlak syndrome 2 for gene: AP3B1","entity_name":"AP3B1","entity_type":"gene"},{"created":"2020-08-27T20:59:16.231946+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hyaline fibromatosis syndrome for gene: ANTXR2","entity_name":"ANTXR2","entity_type":"gene"},{"created":"2020-08-27T20:59:15.938806+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 2L for gene: ANO5","entity_name":"ANO5","entity_type":"gene"},{"created":"2020-08-27T20:59:15.657782+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, autosomal recessive 10 for gene: ANO10","entity_name":"ANO10","entity_type":"gene"},{"created":"2020-08-27T20:59:15.344702+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Thrombocytopenia 2 for gene: ANKRD26","entity_name":"ANKRD26","entity_type":"gene"},{"created":"2020-08-27T20:59:15.057279+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Craniometaphyseal dysplasia for gene: ANKH","entity_name":"ANKH","entity_type":"gene"},{"created":"2020-08-27T20:59:14.751069+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Spherocytosis for gene: ANK1","entity_name":"ANK1","entity_type":"gene"},{"created":"2020-08-27T20:59:14.520436+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hyperglycinaemia, non-ketotic for gene: AMT","entity_name":"AMT","entity_type":"gene"},{"created":"2020-08-27T20:59:14.226100+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, Norwegian type for gene: AMN","entity_name":"AMN","entity_type":"gene"},{"created":"2020-08-27T20:59:13.931037+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Amelogenesis imperfecta for gene: AMELX","entity_name":"AMELX","entity_type":"gene"},{"created":"2020-08-27T20:59:13.329338+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Parietal foramina 2 for gene: ALX4","entity_name":"ALX4","entity_type":"gene"},{"created":"2020-08-27T20:59:13.036757+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Amyotrophic lateral sclerosis for gene: ALS2","entity_name":"ALS2","entity_type":"gene"},{"created":"2020-08-27T20:59:12.734644+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hypophosphatasia for gene: ALPL","entity_name":"ALPL","entity_type":"gene"},{"created":"2020-08-27T20:59:12.439925+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: ALOXE3","entity_name":"ALOXE3","entity_type":"gene"},{"created":"2020-08-27T20:59:12.145465+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: ALOX12B","entity_name":"ALOX12B","entity_type":"gene"},{"created":"2020-08-27T20:59:11.849898+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Alstrom syndrome for gene: ALMS1","entity_name":"ALMS1","entity_type":"gene"},{"created":"2020-08-27T20:59:11.553396+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 disorder of glycosylation, type Ih for gene: ALG8","entity_name":"ALG8","entity_type":"gene"},{"created":"2020-08-27T20:59:11.318714+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 disorder of glycosylation, type Ic for gene: ALG6","entity_name":"ALG6","entity_type":"gene"},{"created":"2020-08-27T20:59:11.028205+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 disorder of glycosylation, type Id for gene: ALG3","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-08-27T20:59:10.728127+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 disorder of glycosylation, type Ig for gene: ALG12","entity_name":"ALG12","entity_type":"gene"},{"created":"2020-08-27T20:59:10.151966+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 disorder of glycosylation, type Ik for gene: ALG1","entity_name":"ALG1","entity_type":"gene"},{"created":"2020-08-27T20:59:09.856840+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fructose intolerance for gene: ALDOB","entity_name":"ALDOB","entity_type":"gene"},{"created":"2020-08-27T20:59:09.618730+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Succinic semialdehyde dehydrogenase deficiency for gene: ALDH5A1","entity_name":"ALDH5A1","entity_type":"gene"},{"created":"2020-08-27T20:59:09.324632+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Sjogren-Larsson syndrome for gene: ALDH3A2","entity_name":"ALDH3A2","entity_type":"gene"},{"created":"2020-08-27T20:59:09.034513+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cutis laxa, autosomal recessive, type IIIA for gene: ALDH18A1","entity_name":"ALDH18A1","entity_type":"gene"},{"created":"2020-08-27T20:59:08.736033+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Analbuminemia for gene: ALB","entity_name":"ALB","entity_type":"gene"},{"created":"2020-08-27T20:59:08.442253+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, sideroblastic, X-linked for gene: ALAS2","entity_name":"ALAS2","entity_type":"gene"},{"created":"2020-08-27T20:59:08.146100+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Bile acid synthesis defect, congenital, 2 for gene: AKR1D1","entity_name":"AKR1D1","entity_type":"gene"},{"created":"2020-08-27T20:59:07.631102+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia for gene: AIRE","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-08-27T20:59:07.338834+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cowchock syndrome for gene: AIFM1","entity_name":"AIFM1","entity_type":"gene"},{"created":"2020-08-27T20:59:07.060257+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-3 for gene: AHI1","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-08-27T20:59:06.742112+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hyperoxaluria, primary, type 1 for gene: AGXT","entity_name":"AGXT","entity_type":"gene"},{"created":"2020-08-27T20:59:06.447055+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Myasthenia, limb-girdle, familial for gene: AGRN","entity_name":"AGRN","entity_type":"gene"},{"created":"2020-08-27T20:59:06.140867+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Glycogen storage disease IIIa for gene: AGL","entity_name":"AGL","entity_type":"gene"},{"created":"2020-08-27T20:59:05.847425+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Aspartylglucosaminuria for gene: AGA","entity_name":"AGA","entity_type":"gene"},{"created":"2020-08-27T20:59:05.549727+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hypermethioninemia due to adenosine kinase deficiency for gene: ADK","entity_name":"ADK","entity_type":"gene"},{"created":"2020-08-27T20:59:05.317443+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene ADAR was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nAdded phenotypes Dyschromatosis symmetrica hereditaria for gene: ADAR","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-08-27T20:59:04.751436+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene ADAR was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes Aicardi-Goutieres syndrome for gene: ADAR","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-08-27T20:59:04.450384+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Geleophysic dysplasia 1 for gene: ADAMTSL2","entity_name":"ADAMTSL2","entity_type":"gene"},{"created":"2020-08-27T20:59:04.147656+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Thrombotic thrombocytopenic purpura, familial for gene: ADAMTS13","entity_name":"ADAMTS13","entity_type":"gene"},{"created":"2020-08-27T20:59:03.854242+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 due to ADA deficiency for gene: ADA","entity_name":"ADA","entity_type":"gene"},{"created":"2020-08-27T20:59:03.555756+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Telangiectasia, hereditary hemorrhagic, type 2 for gene: ACVRL1","entity_name":"ACVRL1","entity_type":"gene"},{"created":"2020-08-27T20:59:03.248532+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fibrodysplasia ossificans progressiva for gene: ACVR1","entity_name":"ACVR1","entity_type":"gene"},{"created":"2020-08-27T20:59:02.955469+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Glomerulosclerosis, focal segmental, 1 for gene: ACTN4","entity_name":"ACTN4","entity_type":"gene"},{"created":"2020-08-27T20:59:02.717436+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Macrothrombocytopenia for gene: ACTN1","entity_name":"ACTN1","entity_type":"gene"},{"created":"2020-08-27T20:59:02.424869+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Megacystis-microcolon-intestinal hypoperistalsis syndrome for gene: ACTG2","entity_name":"ACTG2","entity_type":"gene"},{"created":"2020-08-27T20:59:02.126954+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Baraitser-Winter syndrome for gene: ACTG1","entity_name":"ACTG1","entity_type":"gene"},{"created":"2020-08-27T20:59:01.540738+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 dominant for gene: ACTG1","entity_name":"ACTG1","entity_type":"gene"},{"created":"2020-08-27T20:59:01.243578+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Baraitser-Winter syndrome for gene: ACTB","entity_name":"ACTB","entity_type":"gene"},{"created":"2020-08-27T20:59:00.941653+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: ACTA1","entity_name":"ACTA1","entity_type":"gene"},{"created":"2020-08-27T20:59:00.646784+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Combined malonic and methylmalonic aciduria for gene: ACSF3","entity_name":"ACSF3","entity_type":"gene"},{"created":"2020-08-27T20:59:00.351805+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Peroxisomal acyl-CoA oxidase deficiency for gene: ACOX1","entity_name":"ACOX1","entity_type":"gene"},{"created":"2020-08-27T20:59:00.092235+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Renal tubular dysgenesis for gene: ACE","entity_name":"ACE","entity_type":"gene"},{"created":"2020-08-27T20:58:59.751994+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Alpha-methylacetoacetic aciduria for gene: ACAT1","entity_name":"ACAT1","entity_type":"gene"},{"created":"2020-08-27T20:58:59.453340+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes VLCAD deficiency for gene: ACADVL","entity_name":"ACADVL","entity_type":"gene"},{"created":"2020-08-27T20:58:59.218866+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Medium chain acyl CoA dehydrogenase deficiency for gene: ACADM","entity_name":"ACADM","entity_type":"gene"},{"created":"2020-08-27T20:58:58.923524+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes ACAD9 deficiency for gene: ACAD9","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-08-27T20:58:58.347368+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Isobutyryl-CoA dehydrogenase deficiency for gene: ACAD8","entity_name":"ACAD8","entity_type":"gene"},{"created":"2020-08-27T20:58:58.053873+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Sitosterolemia for gene: ABCG5","entity_name":"ABCG5","entity_type":"gene"}]}