Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1414
Gene Symbol: CRYBB1
CRYBB1
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 Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 4810
Gene Symbol: NHS
NHS
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: 1409
Gene Symbol: CRYAA
CRYAA
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.320 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.320 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 1415
Gene Symbol: CRYBB2
CRYBB2
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 1410
Gene Symbol: CRYAB
CRYAB
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 1411
Gene Symbol: CRYBA1
CRYBA1
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 79443
Gene Symbol: FYCO1
FYCO1
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.300 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014
Entrez Id: 146862
Gene Symbol: UNC45B
UNC45B
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.300 GermlineCausalMutation ORPHANET The myosin chaperone UNC45B is involved in lens development and autosomal dominant juvenile cataract. 24549050

2014
Entrez Id: 4810
Gene Symbol: NHS
NHS
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.400 GermlineCausalMutation ORPHANET Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS gene. 24968223

2014
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.320 GermlineCausalMutation ORPHANET A Novel Insertion Variant of CRYGD Is Associated with Congenital Nuclear Cataract in a Chinese Family. 26147294

2015
Entrez Id: 1410
Gene Symbol: CRYAB
CRYAB
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.310 GermlineCausalMutation ORPHANET Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis). 26622071

2015