1. Genes and Genomic Entities
  2. POMZP3

POMZP3

POM121 and ZP3 fusion
OMIM: 600587, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red POMZP3 in Retinal disorders

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 5.4
Latest signed off version: v5.0 (1 May 2024)

review Not set
Sources
  • NHS GMS
  • Literature
Phenotypes
  • Cone dystrophy