Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.320 GeneticVariation disease BEFREE A novel missense mutation in LIM2 is responsible for autosomal recessive congenital cataracts. 27814360 2016
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.320 Biomarker disease BEFREE This study shows the involvement of LIM2 in human congenital cataract. 18596884 2008
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.320 Biomarker disease MGD Identification of a mutation in the MP19 gene, Lim2, in the cataractous mouse mutant To3. 9238094 1997
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.320 Biomarker disease MGD Two new cataract loci, Ccw and To3, and further mapping of the Npp and Opj cataracts in the mouse. 8812411 1996
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.320 CausalMutation disease CLINVAR