PDX1, pancreatic and duodenal homeobox 1, 3651

N. diseases: 185; N. variants: 22
Disease: Pancreatic Agenesis, Congenital ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1850096
Disease: Pancreatic Agenesis, Congenital
Pancreatic Agenesis, Congenital 		0.500 GermlineCausalMutation disease ORPHANET Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence. 8988180 1997
CUI: C1850096
Disease: Pancreatic Agenesis, Congenital
Pancreatic Agenesis, Congenital 		0.500 Biomarker disease CTD_human