CAPN5

calpain 5
OMIM: 602537, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green CAPN5 in Retinal disorders

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 2.285
Latest signed off version: v2.195 (5 Aug 2021)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Genetic Retinal Degeneration Conditions