1. Genes and Genomic Entities
  2. MYO1A

MYO1A

myosin IA
OMIM: 601478, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list MYO1A 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 MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Removed
    • Radboud University Medical Center, Nijmegen
    • Expert
    • Emory Genetics Laboratory
    • UKGTN
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • hearing loss
    • Nonsyndromic Hearing Loss, Dominant
    • Deafness, autosomal dominant 48, 607841
    • Deafness,autosomaldominant48,607841
    Tags
    • curated_removed