OSBPL2

oxysterol binding protein like 2
OMIM: 606731, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Green OSBPL2 in Monogenic hearing loss Level 2: Audiology Version 6.10 Latest signed off version: v6.0 (6 May 2026) Component of the following Super Panels: Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Radboud University Medical Center, Nijmegen Phenotypes #616340: Deafness, autosomal dominant 67 [Hearing loss, sensorineural, mild to profound, Tinnitus at onset of high-frequency hearing loss, No vestibular symptoms]

Panel

Reviews

Mode of inheritance

Details

Level 2: Audiology
Version 6.10
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

Paediatric disorders

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

#616340: Deafness, autosomal dominant 67 [Hearing loss, sensorineural, mild to profound, Tinnitus at onset of high-frequency hearing loss, No vestibular symptoms]