Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content
HuGE Navigator|Genopedia|PHGKB

Genopedia


We have to retire this site due to some reasons. This site has not longer been updated and some links are not working properly.
PRPH2

13 disease terms (MeSH) has been reported with PRPH2 gene.

[Click Sort to re-sort the table]
Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Retinitis Pigmentosa Phenopedia 9 0
    Retinal Dystrophies Phenopedia 3 0
    Vitelliform Macular Dystrophy Phenopedia 3 0
    Disease Progression Phenopedia 2 0
    Macular Degeneration Phenopedia 2 0
    Retinal Degeneration Phenopedia 2 0
    Retinal Diseases Phenopedia 1 0
    Retinal Drusen Phenopedia 1 0
    Myopia Phenopedia 1 0
    Respiratory Distress Syndrome, Newborn Phenopedia 1 0
    Birth Weight Phenopedia 1 0
    Leber Congenital Amaurosis Phenopedia 1 0
    Vision Disorders Phenopedia 1 0
Note: The number of publications displayed in this table will differ from the number displayed in the HuGE Literature Finder as the number in Genopedia reflects only the indexed disease term without children terms, but the number in the HuGE Literature Finder reflects all text searches of the disease term including the indexed term and corresponding children terms.
TOP