Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.320 GeneticVariation BEFREE Overall, mutations in COL11A1 (82.5%) and COL11A2 (94.1%) seem to be more frequently associated with hearing impairment than mutations in COL2A1 (52.2%). 23110709

2012
Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.320 Biomarker BEFREE Evaluation of hearing impairment as a feature of the nonocular Stickler syndrome (type II) linked to COL11A2. 10718438

2000
Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.320 Biomarker GENOMICS_ENGLAND Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome). 9805126

1998