RNLS

renalase, FAD dependent amine oxidase
OMIM: 609360, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red RNLS in Bilateral congenital or childhood onset cataracts

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 4.12
Latest signed off version: v4.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Congenital cataract, autosomal recessive