GPC5, glypican 5, 2262

N. diseases: 65; N. variants: 20
Disease: Abnormality of digit ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3550704
Disease: Abnormality of digit
Abnormality of digit 		0.010 Biomarker phenotype BEFREE Microdeletions leading to haploinsufficiency of miR17∼92, a cluster of micro RNA genes closely linked to GPC5 in both mouse and human genomes, has recently been associated with digital anomalies in the Feingold like syndrome. 23792790 2013