IRX6

iroquois homeobox 6
OMIM: 606196, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber IRX6 in Mendeliome


Version 2.0

2 reviews 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 1.0

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