Genomics England
GMS Panels
Panels
Genes and Entities
RD3
retinal degeneration 3
OMIM:
180040
See this entity in PanelApp
Panel
Mode of inheritance
Details
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1 panel
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in
Retinal disorders
R-numbers:
R32
Signed-off version 6.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Leber Congenital Amaurosis, Leber congenital amaurosis 12, 610612, Eye Disorders