Genomics England
GMS Panels
Panels
Genes and Entities

MPZL2

myelin protein zero like 2
OMIM: 604873
PanelMode of inheritanceDetails
1 panel
Green
in Monogenic hearing loss
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.57
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Deafness, autosomal recessive 111, OMIM:618145, deafness, autosomal recessive 111, MONDO:0029142