Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26160
Gene Symbol: IFT172
IFT172
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.410 GermlineCausalMutation ORPHANET Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome. 25168386

2015