IRX6

iroquois homeobox 6
OMIM: 606196, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber IRX6 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • cone dystrophy, MONDO:0000455

Amber IRX6 in Cone-rod Dystrophy


Level 2: Ophthalmological disorders
Version 0.54

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • cone dystrophy, MONDO:0000455
    Tags
    • SV/CNV