EGFLAM

EGF like, fibronectin type III and laminin G domains
OMIM: 617683, Gene2Phenotype

1 panel

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


Level 2: Ophthalmology
Version 9.3
Latest signed off version: v9.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Congenital stationary night blindness, HP:0007642
Tags
  • Q4_25_promote_green
  • Q4_25_NHS_review