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Mammalian Phenotype Browser
Term Detail
MP term:retinal degeneration
MP id: MP:0001326
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
Number of paths to term: 1

is-adenotes an 'is-a' relationship
part-ofdenotes a 'part-of' relationship


mammalian phenotype
        is-avision/eye phenotype
                is-aabnormal eye morphology
                        is-aabnormal posterior eye segment morphology
                                is-aabnormal ocular fundus morphology
                                        is-aabnormal retina morphology
                                                is-aabnormal amacrine cell morphology +
                                                is-aabnormal horizontal cell morphology +
                                                is-aabnormal Muller cell morphology
                                                is-aabnormal retina inner limiting membrane morphology
                                                is-aabnormal retina outer limiting membrane morphology
                                                is-aabnormal retinal bipolar cell morphology +
                                                is-aabnormal retinal development +
                                                is-aabnormal retinal layer morphology +
                                                is-aabnormal retinal vasculature morphology +
                                                is-aabnormal total retina thickness +
                                                is-aabsent retina
                                                is-adecreased susceptibility to induced retinal damage
                                                is-adecreased ventral retina size
                                                is-aretina coloboma
                                                is-aretina hyperplasia
                                                is-aretina hypoplasia
                                                is-aretinal degeneration [MP:0001326] (215 genotypes, 215 annotations)
                                                is-aretinal deposits +
                                                is-aretinal detachment
                                                is-aretinal fibrosis
                                                is-aretinal gliosis
                                                is-aretinal hemorrhage
                                                is-aretinal spots

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last database update
10/21/2014
MGI 5.20
The Jackson Laboratory