CRYAB, crystallin alpha B, 1410

N. diseases: 200; N. variants: 30
Disease: Nuclear non-senile cataract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 GermlineCausalMutation disease ORPHANET Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis). 26622071 2015
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 GermlineCausalMutation disease ORPHANET Molecular genetics of congenital nuclear cataract. 24384146 2014
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 GermlineCausalMutation disease ORPHANET A novel mutation in CRYAB associated with autosomal dominant congenital nuclear cataract in a Chinese family. 19597569 2009
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 Biomarker disease BEFREE Evidence for the participation of alpha B-crystallin in human age-related nuclear cataract. 9650087 1998