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Date	Panel	Item	Activity
Filter activities 6 actions
08 Feb 2021	Infantile enterocolitis & monogenic inflammatory bowel disease v1.19	G6PC3	Sarah Leigh Phenotypes for gene: G6PC3 were changed from Congenital neutropenia to Dursun syndrome OMIM:612541; Neutropenia, severe congenital 4, autosomal recessive OMIM:612541; autosomal recessive severe congenital neutropenia due to G6PC3 deficiency MONDO:0012930
13 Oct 2016	Infantile enterocolitis & monogenic inflammatory bowel disease	G6PC3	Richard Scott classified G6PC3 as green
13 Oct 2016	Infantile enterocolitis & monogenic inflammatory bowel disease	G6PC3	Richard Scott commented on G6PC3
12 Oct 2016	Infantile enterocolitis & monogenic inflammatory bowel disease	G6PC3	Ellen McDonagh classified G6PC3 as amber
12 Oct 2016	Infantile enterocolitis & monogenic inflammatory bowel disease	G6PC3	Ellen McDonagh commented on G6PC3
12 Oct 2016	Infantile enterocolitis & monogenic inflammatory bowel disease	G6PC3	Neil shah reviewed G6PC3