Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3815
Gene Symbol: KIT
KIT
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.020 Biomarker BEFREE Thus, the finding of a piebald subject with a mutation that impairs receptor activity strongly implicates the c-kit gene in the molecular pathogenesis of this human developmental defect. 1376329

1992
Entrez Id: 3815
Gene Symbol: KIT
KIT
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.020 Biomarker BEFREE Deletion of the c-kit protooncogene in the human developmental defect piebald trait. 1720553

1991