MIP, major intrinsic protein of lens fiber, 4284

N. diseases: 181; N. variants: 21
Disease: Embryonal nuclear cataract (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		0.110 Biomarker disease HPO
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		0.110 GeneticVariation disease BEFREE A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family. 21647270 2011