WBP2

WW domain binding protein 2
OMIM: 606962, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber WBP2 in Monogenic hearing loss Level 3: Non-syndromic hearing loss Level 2: Hearing and ear disorders Version 4.41 Latest signed off version: v4.39 (1 May 2024) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Deafness, autosomal recessive 107, 617639

Panel

Reviews

Mode of inheritance

Details

Amber WBP2 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.41
Latest signed off version: v4.39 (1 May 2024)

Component of the following Super Panels:

Paediatric disorders

review

BIALLELIC, autosomal or pseudoautosomal

Sources

Expert Review Amber
Expert list

Phenotypes

Deafness, autosomal recessive 107, 617639