CLRN2

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber CLRN2 in Monogenic hearing loss Level 3: Non-syndromic hearing loss Level 2: Hearing and ear disorders Version 4.38 Latest signed off version: v4.0 (22 Mar 2023) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes ?Deafness, autosomal recessive 117, OMIM:619174 deafness, autosomal recessive 117, MONDO:0030905

Panel

Reviews

Mode of inheritance

Details

Amber CLRN2 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.38
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

Paediatric disorders

review

BIALLELIC, autosomal or pseudoautosomal

Sources

Expert Review Amber
Literature

Phenotypes

?Deafness, autosomal recessive 117, OMIM:619174
deafness, autosomal recessive 117, MONDO:0030905