Activity

Filter

Panel

Version

Gene or Genomic Entity Name

Date from

Date to

Cancel

Date	Panel	Item	Activity
Filter activities 4 actions
03 Nov 2021	Monogenic hearing loss v2.208	EDN3	Ivone Leong Added comment: Comment on mode of inheritance: MOI changed from "BOTH monoallelic and biallelic, autosomal or pseudoautosomal" to "BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal" as patients with biallelic variants have a more severe phenotype. This MOI change does not affect tiering.
03 Nov 2021	Monogenic hearing loss v2.208	EDN3	Ivone Leong Mode of inheritance for gene: EDN3 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
11 Oct 2018	Monogenic hearing loss v1.43	EDN3	Ellen McDonagh commented on gene: EDN3: New review confirms gene status and mode of inheritance; no changes required.
10 Apr 2018	Monogenic hearing loss	EDN3	Lampros Mavrogiannis reviewed EDN3