EPS8L2

EPS8 like 2
OMIM: 614988, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green EPS8L2 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 Green
    • Expert list
    Phenotypes
    • Deafness, autosomal recessive 106, OMIM:617637