Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4284
Gene Symbol: MIP
MIP
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.400 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 4284
Gene Symbol: MIP
MIP
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.400 GermlineCausalMutation ORPHANET A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family. 21647270

2011
Entrez Id: 4284
Gene Symbol: MIP
MIP
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.400 GermlineCausalMutation ORPHANET A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family. 21245956

2011