Gene: FKBP10 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10 		0.300 GermlineCausalMutation disease ORPHANET Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations. 23712425 2013