C19orf44

chromosome 19 open reading frame 44
ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green C19orf44 in Mendeliome


Version 1.3795

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Late onset retinal dystrophy
  • MONDO:0019118

Green C19orf44 in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 0.225

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Late onset retinal dystrophy, MONDO:0019118