C19orf44

chromosome 19 open reading frame 44
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber C19orf44 in Retinal disorders


Level 2: Ophthalmology
Version 8.86
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Research
Phenotypes
  • late onset retinal dystrophy
Tags
  • Q1_25_ NHS_review
  • Q1_25_ promote_green