Genomics England
GMS Panels
Panels
Genes and Entities
CAPN5
calpain 5
OMIM:
602537
See this entity in PanelApp
Panel
Mode of inheritance
Details
Filter panels
1 panel
Green
in
Retinal disorders
R-numbers:
R32
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Genetic Retinal Degeneration Conditions