XXYLT1

xyloside xylosyltransferase 1
OMIM: 614552, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber XXYLT1 in Mendeliome


Version 2.516

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Inherited retinal dystrophy, MONDO:0019118, XXYLT1-related
Tags
  • founder

Amber XXYLT1 in Macular Dystrophy/Stargardt Disease


Level 2: Ophthalmological disorders
Version 1.2

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • Inherited retinal dystrophy, MONDO:0019118, XXYLT1-related
    Tags
    • founder