Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Mitochondrial disorders v1.461 IDH3B Sarah Leigh Mode of inheritance for gene: IDH3B was changed from to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v1.123 IDH3B Ellen McDonagh Phenotypes for gene: IDH3B were changed from to Retinitis pigmentosa 46, 612572
Mitochondrial disorders v1.122 IDH3B Ellen McDonagh Publications for gene: IDH3B were set to
Mitochondrial disorders v1.121 IDH3B Ellen McDonagh Classified gene: IDH3B as Amber List (moderate evidence)
Mitochondrial disorders v1.121 IDH3B Ellen McDonagh Added comment: Comment on list classification: This gene-disease was discussed on the NHSE GMS Mitochondrial Specialist Group Meeting call on 25th February 2019, and the decision was made to make this gene Amber.
Mitochondrial disorders v1.121 IDH3B Ellen McDonagh Gene: idh3b has been classified as Amber List (Moderate Evidence).
Mitochondrial disorders IDH3B Zornitza Stark reviewed gene: IDH3B
Mitochondrial disorders IDH3B Sarah Leigh Added gene to panel