CRYGC, crystallin gamma C, 1420

N. diseases: 60; N. variants: 13
Disease: Cataract microcornea syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		0.300 GermlineCausalMutation disease ORPHANET A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree. 22876111 2012
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		0.300 GermlineCausalMutation disease ORPHANET A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea. 19204787 2009