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Date	Panel	Item	Activity
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03 Nov 2021	Monogenic hearing loss v2.209	EDNRB	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 v2.209	EDNRB	Ivone Leong Mode of inheritance for gene: EDNRB 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	EDNRB	Ellen McDonagh commented on gene: EDNRB: New review confirms gene status and mode of inheritance; no changes required.
10 Apr 2018	Monogenic hearing loss	EDNRB	Lampros Mavrogiannis reviewed EDNRB