MPZL2

myelin protein zero like 2
OMIM: 604873, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green MPZL2 in Hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 2.247
Latest signed off version: v2.5 (13 Feb 2020)

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