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 6.184
Latest signed off version: v6.0 (30 Apr 2025)

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


Level 2: Audiology
Version 5.63
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert