VIM, vimentin, 7431

N. diseases: 644; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3805411
Disease: CATARACT 30
CATARACT 30
0.800 GeneticVariation disease UNIPROT Targeted Exome Sequencing of Congenital Cataracts Related Genes: Broadening the Mutation Spectrum and Genotype-Phenotype Correlations in 27 Chinese Han Families. 28450710 2017
CUI: C3805411
Disease: CATARACT 30
CATARACT 30
0.800 GeneticVariation disease UNIPROT Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing. 26694549 2016
CUI: C3805411
Disease: CATARACT 30
CATARACT 30
0.800 Biomarker disease GENOMICS_ENGLAND Defect of mitotic vimentin phosphorylation causes microophthalmia and cataract via aneuploidy and senescence in lens epithelial cells. 24142690 2013
CUI: C3805411
Disease: CATARACT 30
CATARACT 30
0.800 GeneticVariation disease UNIPROT Dominant cataract formation in association with a vimentin assembly disrupting mutation. 19126778 2009
CUI: C3805411
Disease: CATARACT 30
CATARACT 30
0.800 CausalMutation disease CLINVAR
CUI: C3805411
Disease: CATARACT 30
CATARACT 30
0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C3805411
Disease: CATARACT 30
CATARACT 30
0.800 Biomarker disease MGD