ROR1

receptor tyrosine kinase like orphan receptor 1
OMIM: 602336, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber ROR1 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 Amber
    • Expert list
    Phenotypes
    • Deafness, autosomal recessive 108, MIM#617654
    • deafness, autosomal recessive 108 MONDO:0033200