EPHA10

EPH receptor A10
OMIM: 611123, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red EPHA10 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	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Phenotypes postlingual non-syndromic genetic hearing loss, MONDO:0016298

Panel

Reviews

Mode of inheritance

Details

Red EPHA10 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

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Sources

Literature

Phenotypes

postlingual non-syndromic genetic hearing loss, MONDO:0016298