| 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 |
denotes an 'is-a' relationship
denotes a 'part-of' relationship
vision/eye phenotypeabnormal eye morphologyabnormal posterior eye segment morphologyabnormal ocular fundus morphologyabnormal retina morphologyabnormal amacrine cell morphology +abnormal horizontal cell morphology +abnormal Muller cell morphologyabnormal retina inner limiting membrane morphologyabnormal retina outer limiting membrane morphologyabnormal retinal bipolar cell morphology +abnormal retinal development +abnormal retinal layer morphology +abnormal retinal vasculature morphology +abnormal total retina thickness +absent retinadecreased susceptibility to induced retinal damagedecreased ventral retina sizeretina colobomaretina hyperplasiaretina hypoplasiaretinal degeneration [MP:0001326] (200 genotypes, 200 annotations)retinal deposits +retinal detachmentretinal fibrosisretinal gliosisretinal hemorrhageMouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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