MIP, major intrinsic protein of lens fiber, 4284

N. diseases: 181; N. variants: 21
Disease: Cataract, Central Saccular, With Sutural Opacities ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1854021
Disease: Cataract, Central Saccular, With Sutural Opacities
Cataract, Central Saccular, With Sutural Opacities 		0.300 GermlineCausalMutation disease ORPHANET A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family. 24405844 2014
CUI: C1854021
Disease: Cataract, Central Saccular, With Sutural Opacities
Cataract, Central Saccular, With Sutural Opacities 		0.300 GermlineCausalMutation disease ORPHANET A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family. 20361015 2010