DDR1

discoidin domain receptor tyrosine kinase 1
OMIM: 600408, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber DDR1 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.5
Latest signed off version: v7.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
Phenotypes
  • Chondrodysplasia with multiple dislocations
Red DDR1 in Monogenic hearing loss


Level 2: Audiology
Version 6.10
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert