{"count":220497,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=94","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=92","results":[{"created":"2025-12-11T11:39:57.306404+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.148","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PAX6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"PAX6","entity_type":"gene"},{"created":"2025-12-11T11:39:49.003134+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.148","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene PAX6 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:39:04.611920+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.147","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: NODAL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"NODAL","entity_type":"gene"},{"created":"2025-12-11T11:38:49.708142+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.147","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene NODAL from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:37:37.593222+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.146","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: HNRNPU: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"HNRNPU","entity_type":"gene"},{"created":"2025-12-11T11:37:28.099790+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.146","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene HNRNPU from panel Intellectual disability syndromic and non-syndromic","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:37:21.119828+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.496","user_name":"Chirag Patel","item_type":"entity","text":"Deleted their review","entity_name":"HNRNPU","entity_type":"gene"},{"created":"2025-12-11T11:37:18.634830+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.496","user_name":"Chirag Patel","item_type":"entity","text":"Deleted their comment","entity_name":"HNRNPU","entity_type":"gene"},{"created":"2025-12-11T11:36:54.867753+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.496","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: HNRNPU: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"HNRNPU","entity_type":"gene"},{"created":"2025-12-11T11:36:26.378051+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3766","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene HHIP from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:36:06.497816+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.145","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: HHIP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"HHIP","entity_type":"gene"},{"created":"2025-12-11T11:28:10.693578+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.145","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: GPR161 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GPR161","entity_type":"gene"},{"created":"2025-12-11T11:27:41.506694+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.144","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene GPR161 from panel Growth failure","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:27:15.840186+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.143","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: GHRH: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"GHRH","entity_type":"gene"},{"created":"2025-12-11T11:24:59.109617+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.143","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: FOXH1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FOXH1","entity_type":"gene"},{"created":"2025-12-11T11:24:03.630797+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.143","user_name":"Chirag Patel","item_type":"entity","text":"commented on gene: BMP2","entity_name":"BMP2","entity_type":"gene"},{"created":"2025-12-11T11:15:37.300772+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.143","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HFE2 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:15:37.246949+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.143","user_name":"Chirag Patel","item_type":"entity","text":"gene: HFE2 was added\ngene: HFE2 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nnew gene name tags were added to gene: HFE2.\nMode of inheritance for gene: HFE2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HFE2 were set to Hemochromatosis, type 2A, MIM# 602390","entity_name":"HFE2","entity_type":"gene"},{"created":"2025-12-11T11:15:31.795166+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.142","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HFE from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:15:31.713045+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.142","user_name":"Chirag Patel","item_type":"entity","text":"gene: HFE was added\ngene: HFE was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HFE was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HFE were set to Haemochromatosis, MIM# 235200","entity_name":"HFE","entity_type":"gene"},{"created":"2025-12-11T11:15:25.658940+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.141","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HAMP from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:15:25.585820+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.141","user_name":"Chirag Patel","item_type":"entity","text":"gene: HAMP was added\ngene: HAMP was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HAMP was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HAMP were set to 12469120; 34828384; 15198949\nPhenotypes for gene: HAMP were set to Haemochromatosis, type 2B, MIM# 613313","entity_name":"HAMP","entity_type":"gene"},{"created":"2025-12-11T11:15:16.862157+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.140","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene GNRH1 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:15:16.791981+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.140","user_name":"Chirag Patel","item_type":"entity","text":"gene: GNRH1 was added\ngene: GNRH1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GNRH1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GNRH1 were set to 19535795; 19567835; 32134721; 31200363; 26595427\nPhenotypes for gene: GNRH1 were set to Hypogonadotropic hypogonadism 12 with or without anosmia, MIM# 614841","entity_name":"GNRH1","entity_type":"gene"},{"created":"2025-12-11T11:15:11.388971+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.139","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene FSHB from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:15:11.313576+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.139","user_name":"Chirag Patel","item_type":"entity","text":"gene: FSHB was added\ngene: FSHB was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: FSHB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FSHB were set to 8220432; 9280841; 9624193; 9806482; 9271483; 16630814\nPhenotypes for gene: FSHB were set to Hypogonadotropic hypogonadism 24 without anosmia, MIM#229070","entity_name":"FSHB","entity_type":"gene"},{"created":"2025-12-11T11:15:04.260636+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.138","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene FLRT3 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:15:04.185419+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.138","user_name":"Chirag Patel","item_type":"entity","text":"gene: FLRT3 was added\ngene: FLRT3 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red,Expert Review Red,Victorian Clinical Genetics Services\nMode of inheritance for gene: FLRT3 was set to Unknown\nPublications for gene: FLRT3 were set to 23643382; 31200363\nPhenotypes for gene: FLRT3 were set to Hypogonadotropic hypogonadism 21 with anosmia (MIM# 615271)","entity_name":"FLRT3","entity_type":"gene"},{"created":"2025-12-11T11:14:57.859886+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.137","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene FGF17 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:57.788534+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.137","user_name":"Chirag Patel","item_type":"entity","text":"gene: FGF17 was added\ngene: FGF17 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FGF17 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: FGF17 were set to 23643382; 31748124","entity_name":"FGF17","entity_type":"gene"},{"created":"2025-12-11T11:14:52.395105+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.136","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene FEZF1 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:52.355989+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.136","user_name":"Chirag Patel","item_type":"entity","text":"gene: FEZF1 was added\ngene: FEZF1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Amber\nMode of inheritance for gene: FEZF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FEZF1 were set to 25192046; 32400067\nPhenotypes for gene: FEZF1 were set to Hypogonadotropic hypogonadism 22, with or without anosmia 616030","entity_name":"FEZF1","entity_type":"gene"},{"created":"2025-12-11T11:14:44.479254+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.135","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene DUSP6 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:44.404396+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.135","user_name":"Chirag Patel","item_type":"entity","text":"gene: DUSP6 was added\ngene: DUSP6 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red\nMode of inheritance for gene: DUSP6 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DUSP6 were set to 23643382; 32389901\nPhenotypes for gene: DUSP6 were set to Hypogonadotropic hypogonadism 19 with or without anosmia - MIM#615269","entity_name":"DUSP6","entity_type":"gene"},{"created":"2025-12-11T11:14:32.193820+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.134","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene DCAF17 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:32.145788+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.134","user_name":"Chirag Patel","item_type":"entity","text":"gene: DCAF17 was added\ngene: DCAF17 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Green,Expert Review Green,Expert Review\nMode of inheritance for gene: DCAF17 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DCAF17 were set to 19026396; 20507343; 35002959; 34877714; 34732557; 34590781\nPhenotypes for gene: DCAF17 were set to Woodhouse-Sakati syndrome, MIM#\t241080","entity_name":"DCAF17","entity_type":"gene"},{"created":"2025-12-11T11:14:26.517693+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.133","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CUL4B from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:26.465685+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.133","user_name":"Chirag Patel","item_type":"entity","text":"gene: CUL4B was added\ngene: CUL4B was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert list,Expert Review Green,Expert Review Green,Expert Review Green,Expert Review Green,Expert list,Victorian Clinical Genetics Services\nMode of inheritance for gene: CUL4B was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: CUL4B were set to PMID: 25385192\nPhenotypes for gene: CUL4B were set to Mental retardation, X-linked, syndromic 15 (Cabezas type)\t300354","entity_name":"CUL4B","entity_type":"gene"},{"created":"2025-12-11T11:14:19.800262+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.132","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CLPP from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:19.752418+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.132","user_name":"Chirag Patel","item_type":"entity","text":"gene: CLPP was added\ngene: CLPP was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Amber,Expert Review Amber,Expert Review\nMode of inheritance for gene: CLPP was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLPP were set to 23541340; 25956234; 26970254; 27087618; 27650058; 27650058; 27899912\nPhenotypes for gene: CLPP were set to Perrault syndrome 3, MIM# 614129","entity_name":"CLPP","entity_type":"gene"},{"created":"2025-12-11T11:14:12.997250+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.131","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CCDC141 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:12.765075+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.131","user_name":"Chirag Patel","item_type":"entity","text":"gene: CCDC141 was added\ngene: CCDC141 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Amber,Expert Review Amber,Expert Review\nMode of inheritance for gene: CCDC141 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: CCDC141 were set to 251920460; 28324054; 32520725; 27014940\nPhenotypes for gene: CCDC141 were set to congenital hypogonadotropic hypogonadism, MONDO:0015770, CCDC141-related","entity_name":"CCDC141","entity_type":"gene"},{"created":"2025-12-11T11:14:06.998661+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.130","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene AXL from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:14:06.952175+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.130","user_name":"Chirag Patel","item_type":"entity","text":"gene: AXL was added\ngene: AXL was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Red,Expert Review Red,Expert Review\nMode of inheritance for gene: AXL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AXL were set to 24476074\nPhenotypes for gene: AXL were set to Hypogonadotropic hypogonadism, MONDO:0018555, AXL-related","entity_name":"AXL","entity_type":"gene"},{"created":"2025-12-11T11:13:59.178246+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.129","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ARHGAP35 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:59.100021+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.129","user_name":"Chirag Patel","item_type":"entity","text":"gene: ARHGAP35 was added\ngene: ARHGAP35 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Expert Review Green,Literature\nMode of inheritance for gene: ARHGAP35 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ARHGAP35 were set to PMID: 36178483\nPhenotypes for gene: ARHGAP35 were set to Hypogonadotropic hypogonadism, MONDO:0015770, ARHGAP35-related","entity_name":"ARHGAP35","entity_type":"gene"},{"created":"2025-12-11T11:13:53.007652+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.128","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ANOS1 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:52.961500+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.128","user_name":"Chirag Patel","item_type":"entity","text":"gene: ANOS1 was added\ngene: ANOS1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ANOS1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: ANOS1 were set to 1594017; 8504298; 8989261\nPhenotypes for gene: ANOS1 were set to Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), MIM# 308700","entity_name":"ANOS1","entity_type":"gene"},{"created":"2025-12-11T11:13:44.610879+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.127","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TFR2 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:44.561625+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.127","user_name":"Chirag Patel","item_type":"entity","text":"gene: TFR2 was added\ngene: TFR2 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TFR2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TFR2 were set to 24847265; 29743178\nPhenotypes for gene: TFR2 were set to Haemochromatosis, type 3 (MIM#604250)","entity_name":"TFR2","entity_type":"gene"},{"created":"2025-12-11T11:13:38.972438+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.126","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TCF12 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:38.898177+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.126","user_name":"Chirag Patel","item_type":"entity","text":"gene: TCF12 was added\ngene: TCF12 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Expert Review Green,Literature\nMode of inheritance for gene: TCF12 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: TCF12 were set to 32620954\nPhenotypes for gene: TCF12 were set to Hypogonadotropic hypogonadism 26 with or without anosmia, MIM# 619718; Kallmann syndrome","entity_name":"TCF12","entity_type":"gene"},{"created":"2025-12-11T11:13:33.576924+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.125","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TACR3 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:33.510787+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.125","user_name":"Chirag Patel","item_type":"entity","text":"gene: TACR3 was added\ngene: TACR3 was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Green,Expert Review Green,Expert list\nMode of inheritance for gene: TACR3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TACR3 were set to 20332248; 19079066\nPhenotypes for gene: TACR3 were set to Hypogonadotropic hypogonadism 11 with or without anosmia, MIM#\t614840","entity_name":"TACR3","entity_type":"gene"},{"created":"2025-12-11T11:13:26.564132+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.124","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TAC3 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:26.496511+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.124","user_name":"Chirag Patel","item_type":"entity","text":"gene: TAC3 was added\ngene: TAC3 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TAC3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TAC3 were set to 19079066; 20332248; 23329188; 22031817\nPhenotypes for gene: TAC3 were set to Hypogonadotropic hypogonadism 10 with or without anosmia (MIM#614839)","entity_name":"TAC3","entity_type":"gene"},{"created":"2025-12-11T11:13:20.311987+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.123","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SPRY4 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:20.267168+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.123","user_name":"Chirag Patel","item_type":"entity","text":"gene: SPRY4 was added\ngene: SPRY4 was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Amber,Expert Review Amber,Expert list\ndisputed tags were added to gene: SPRY4.\nMode of inheritance for gene: SPRY4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SPRY4 were set to 23643382\nPhenotypes for gene: SPRY4 were set to Hypogonadotropic hypogonadism 17 with or without anosmia, MIM#\t615266","entity_name":"SPRY4","entity_type":"gene"},{"created":"2025-12-11T11:13:15.357427+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.122","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SOX10 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:15.290060+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.122","user_name":"Chirag Patel","item_type":"entity","text":"gene: SOX10 was added\ngene: SOX10 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Green,Expert Review\nMode of inheritance for gene: SOX10 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SOX10 were set to 23643381; 15004559\nPhenotypes for gene: SOX10 were set to Kallman syndrome; PCWH syndrome (MIM#609136); Waardenburg syndrome, type 2E, with or without neurologic involvement (MIM#611584); Waardenburg syndrome, type 4C (MIM#613266)\nMode of pathogenicity for gene: SOX10 was set to Other","entity_name":"SOX10","entity_type":"gene"},{"created":"2025-12-11T11:13:08.983961+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.121","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SLC40A1 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:08.899577+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.121","user_name":"Chirag Patel","item_type":"entity","text":"gene: SLC40A1 was added\ngene: SLC40A1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC40A1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SLC40A1 were set to 11431687; 11518736; 15956209; 16351644\nPhenotypes for gene: SLC40A1 were set to Haemochromatosis, type 4, MIM# 606069","entity_name":"SLC40A1","entity_type":"gene"},{"created":"2025-12-11T11:13:02.930925+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.120","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SLC29A3 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:13:02.855708+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.120","user_name":"Chirag Patel","item_type":"entity","text":"gene: SLC29A3 was added\ngene: SLC29A3 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC29A3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC29A3 were set to 18940313; 19336477; 22238637\nPhenotypes for gene: SLC29A3 were set to Histiocytosis-lymphadenopathy plus syndrome, MIM# 602782","entity_name":"SLC29A3","entity_type":"gene"},{"created":"2025-12-11T11:12:55.895386+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.119","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SEMA3F from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:55.850762+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.119","user_name":"Chirag Patel","item_type":"entity","text":"gene: SEMA3F was added\ngene: SEMA3F was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Literature\nMode of inheritance for gene: SEMA3F was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SEMA3F were set to PMID: 33495532\nPhenotypes for gene: SEMA3F were set to Hypogonadotropic hypogonadism","entity_name":"SEMA3F","entity_type":"gene"},{"created":"2025-12-11T11:12:50.159375+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.118","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SEMA3E from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:50.091001+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.118","user_name":"Chirag Patel","item_type":"entity","text":"gene: SEMA3E was added\ngene: SEMA3E was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Red,Expert Review\nMode of inheritance for gene: SEMA3E was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SEMA3E were set to 25985275\nPhenotypes for gene: SEMA3E were set to ?CHARGE syndrome (MIM#214800)","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2025-12-11T11:12:44.296166+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SEMA3A from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:44.251376+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"gene: SEMA3A was added\ngene: SEMA3A was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Green,Expert Review Green,Expert Review\nMode of inheritance for gene: SEMA3A was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal\nPublications for gene: SEMA3A were set to 28075028; 33369061; 20301509; 21059704; 24124006; 22927827\nPhenotypes for gene: SEMA3A were set to Hypogonadotropic hypogonadism 16 with or without anosmia - MIM#614897","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2025-12-11T11:12:37.903343+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PROK2 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:37.853576+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"entity","text":"gene: PROK2 was added\ngene: PROK2 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PROK2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: PROK2 were set to 18559922; 17054399; 17959774; 18285834\nPhenotypes for gene: PROK2 were set to Hypogonadotropic hypogonadism 4 with or without anosmia (MIM#610628)","entity_name":"PROK2","entity_type":"gene"},{"created":"2025-12-11T11:12:30.446870+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PRDM13 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:30.373239+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"entity","text":"gene: PRDM13 was added\ngene: PRDM13 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Amber,Expert Review Amber,Literature\nfounder tags were added to gene: PRDM13.\nMode of inheritance for gene: PRDM13 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PRDM13 were set to 34730112\nPhenotypes for gene: PRDM13 were set to Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, MIM# 619761","entity_name":"PRDM13","entity_type":"gene"},{"created":"2025-12-11T11:12:23.746838+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.114","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PLXNA3 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:23.678130+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.114","user_name":"Chirag Patel","item_type":"entity","text":"gene: PLXNA3 was added\ngene: PLXNA3 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Literature\nMode of inheritance for gene: PLXNA3 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: PLXNA3 were set to PMID: 33495532\nPhenotypes for gene: PLXNA3 were set to Hypogonadotropic hypogonadism","entity_name":"PLXNA3","entity_type":"gene"},{"created":"2025-12-11T11:12:17.182257+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.113","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NSMF from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:17.107363+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.113","user_name":"Chirag Patel","item_type":"entity","text":"gene: NSMF was added\ngene: NSMF was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Red,Expert Review Red,Expert list\nMode of inheritance for gene: NSMF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NSMF were set to 15362570; 17235395; 21700882\nPhenotypes for gene: NSMF were set to Hypogonadotropic hypogonadism 9 with or without anosmia, MIM#\t614838","entity_name":"NSMF","entity_type":"gene"},{"created":"2025-12-11T11:12:10.151949+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NR0B1 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:10.073422+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"gene: NR0B1 was added\ngene: NR0B1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nSV/CNV tags were added to gene: NR0B1.\nMode of inheritance for gene: NR0B1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: NR0B1 were set to 19508677; 26030781\nPhenotypes for gene: NR0B1 were set to Adrenal hypoplasia, congenital (MIM# 300200); 46XY sex reversal 2, dosage-sensitive, MIM#\t300018","entity_name":"NR0B1","entity_type":"gene"},{"created":"2025-12-11T11:12:02.734013+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NHLH2 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:12:02.594735+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"entity","text":"gene: NHLH2 was added\ngene: NHLH2 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Red,Expert Review Red,Expert Review\nMode of inheritance for gene: NHLH2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NHLH2 were set to 35066646\nPhenotypes for gene: NHLH2 were set to Hypogonadotropic hypogonadism 27 without anosmia , MIM#\t619755","entity_name":"NHLH2","entity_type":"gene"},{"created":"2025-12-11T11:11:55.891338+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.110","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NDNF from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:11:55.811948+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.110","user_name":"Chirag Patel","item_type":"entity","text":"gene: NDNF was added\ngene: NDNF was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Amber,Expert Review Amber,Literature\nMode of inheritance for gene: NDNF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NDNF were set to 31883645; 40788466\nPhenotypes for gene: NDNF were set to Hypogonadotropic hypogonadism 25 with anosmia MIM#618841","entity_name":"NDNF","entity_type":"gene"},{"created":"2025-12-11T11:11:46.793084+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene LHB from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:11:46.753933+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"gene: LHB was added\ngene: LHB was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: LHB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: LHB were set to 17761593; 28092701; 29476300; 22723313; 15602022\nPhenotypes for gene: LHB were set to Hypogonadotropic hypogonadism 23 with or without anosmia (MIM#228300)","entity_name":"LHB","entity_type":"gene"},{"created":"2025-12-11T11:11:39.912056+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.108","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene KLB from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:11:39.864908+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.108","user_name":"Chirag Patel","item_type":"entity","text":"gene: KLB was added\ngene: KLB was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Expert Review Green,Literature\nMode of inheritance for gene: KLB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: KLB were set to 28754744\nPhenotypes for gene: KLB were set to Hypogonadotropic hypogonadism","entity_name":"KLB","entity_type":"gene"},{"created":"2025-12-11T11:11:33.993425+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.107","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene KISS1R from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:11:33.948688+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.107","user_name":"Chirag Patel","item_type":"entity","text":"gene: KISS1R was added\ngene: KISS1R was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: KISS1R was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: KISS1R were set to 17164310; 31073722; 14573733\nPhenotypes for gene: KISS1R were set to Hypogonadotropic hypogonadism 8 with or without anosmia (MIM#614837)","entity_name":"KISS1R","entity_type":"gene"},{"created":"2025-12-11T11:11:30.659696+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.106","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene KISS1 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:11:30.595458+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.106","user_name":"Chirag Patel","item_type":"entity","text":"gene: KISS1 was added\ngene: KISS1 was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Amber,Expert Review Amber,Expert list\nMode of inheritance for gene: KISS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: KISS1 were set to 22335740; 25783047; 22766261; 17563351\nPhenotypes for gene: KISS1 were set to Hypogonadotropic hypogonadism 13 with or without anosmia, MIM#\t614842","entity_name":"KISS1","entity_type":"gene"},{"created":"2025-12-11T11:11:18.514146+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene IL17RD from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:11:18.469230+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"entity","text":"gene: IL17RD was added\ngene: IL17RD was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red,Victorian Clinical Genetics Services\ndisputed tags were added to gene: IL17RD.\nMode of inheritance for gene: IL17RD was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: IL17RD were set to 23643382; 32389901\nPhenotypes for gene: IL17RD were set to Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267","entity_name":"IL17RD","entity_type":"gene"},{"created":"2025-12-11T11:11:05.588750+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HS6ST1 from panel Hypogonadotropic hypogonadism","entity_name":null,"entity_type":null},{"created":"2025-12-11T11:11:05.518204+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"entity","text":"gene: HS6ST1 was added\ngene: HS6ST1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red,Expert Review Red,Victorian Clinical Genetics Services\nMode of inheritance for gene: HS6ST1 was set to Other\nPublications for gene: HS6ST1 were set to 21700882\nPhenotypes for gene: HS6ST1 were set to {Hypogonadotropic hypogonadism 15 with or without anosmia} 614880","entity_name":"HS6ST1","entity_type":"gene"},{"created":"2025-12-11T11:09:32.630328+11:00","panel_name":"Hypogonadotropic hypogonadism","panel_id":4521,"panel_version":"0.74","user_name":"Chirag Patel","item_type":"panel","text":"Panel types changed to Victorian Clinical Genetics Services; Genetic Health Queensland; Rare Disease","entity_name":null,"entity_type":null},{"created":"2025-12-11T10:59:12.039291+11:00","panel_name":"Hypogonadotropic hypogonadism","panel_id":4521,"panel_version":"0.73","user_name":"Chirag Patel","item_type":"panel","text":"HPO terms changed from  to Hypogonadotropic hypogonadism HP:0000044\nPanel status changed from internal to public\nPanel types changed to Rare Disease","entity_name":null,"entity_type":null},{"created":"2025-12-11T10:55:34.201657+11:00","panel_name":"Hypogonadotropic hypogonadism","panel_id":4521,"panel_version":"0.72","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene FEZF1 from panel Differences of Sex Development","entity_name":null,"entity_type":null},{"created":"2025-12-11T10:55:34.161476+11:00","panel_name":"Hypogonadotropic hypogonadism","panel_id":4521,"panel_version":"0.72","user_name":"Chirag Patel","item_type":"entity","text":"gene: FEZF1 was added\ngene: FEZF1 was added to Hypogonadotropic hypogonadism. Sources: Expert Review Amber,Victorian Clinical Genetics Services\nMode of inheritance for gene: FEZF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FEZF1 were set to 25192046; 32400067\nPhenotypes for gene: FEZF1 were set to Hypogonadotropic hypogonadism 22, with or without anosmia 616030","entity_name":"FEZF1","entity_type":"gene"}]}