UGT8, UDP glycosyltransferase 8, 7368

N. diseases: 49; N. variants: 3
Disease: PARIETAL FORAMINA ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1868598
Disease: PARIETAL FORAMINA
PARIETAL FORAMINA 		0.010 GeneticVariation disease BEFREE A heterozygous CGT-TGT mutation at codon 672 in SCN4A gene was identified to segregate with the disease in the FPP family. 16386935 2006