Phenotype: retina degeneration

Definition
retrogressive pathological change in the thin layer of neural tissue lining the back of the eyeball, which contains visual receptors and can result in the impairment or cessation of retinal neural function
Synonyms
retinal degeneration
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with retina degeneration

Phenotype associations to genes and alleles will be available once data has completed quality control.

 The way we measure

 Phenotype associations stats

0.00% of tested genes with null mutations on a B6N genetic background have a phenotype association to retina degeneration (0/358)

0.00% females (0/355) 0.00% males (0/356)

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