MYO3A

myosin IIIA
OMIM: 606808, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green MYO3A 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
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • UKGTN
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • Deafness, autosomal recessive 30 OMIM:607101
    • autosomal recessive nonsyndromic deafness 30 MONDO:0011774