PanelApp (test)
  1. Genes and Genomic Entities
  2. RDH11

RDH11

retinol dehydrogenase 11 (all-trans/9-cis/11-cis)
OMIM: 607849, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber RDH11 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Retinal dystrophy, juvenile cataracts, and short stature syndrome, MIM# 616108

Amber RDH11 in Syndromic Retinopathy


Level 2: Ophthalmological disorders
Version 0.209

Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • RetNet
    Phenotypes
    • Retinal dystrophy, juvenile cataracts, and short stature syndrome, MIM# 616108