IRX6

iroquois homeobox 6
OMIM: 606196, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red IRX6 in Retinal disorders


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

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • cone dystrophy, MONDO:0000455
Tags
  • cnv