1. Genes and Genomic Entities
  2. MYO3A

MYO3A

myosin IIIA
OMIM: 606808, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green MYO3A in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.38
Latest signed off version: v4.0 (22 Mar 2023)

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
    Green MYO3A in Severe Paediatric Disorders


    Version 1.184

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Deafness, autosomal recessive 30, 607101