PEX5L

peroxisomal biogenesis factor 5 like
OMIM: 611058, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red PEX5L 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 Unknown
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Peroxisome biogenesis disorder