MPZL2

myelin protein zero like 2
OMIM: 604873, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green MPZL2 in Monogenic hearing loss


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Deafness, autosomal recessive 111, OMIM:618145
    • deafness, autosomal recessive 111, MONDO:0029142