Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 157657
Gene Symbol: C8orf37
C8orf37
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.950 GermlineCausalMutation ORPHANET Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement. 22177090

2012