PROX1, prospero homeobox 1, 5629

N. diseases: 114; N. variants: 10
Disease: Congenital glucose-galactose malabsorption ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268186
Disease: Congenital glucose-galactose malabsorption
Congenital glucose-galactose malabsorption 		0.010 Biomarker disease BEFREE HHEX and PROX1 play significant roles in carbohydrate intolerance and diabetes because these transcription factors may be involved in the regulation of insulin secretion and in glucose and lipid metabolism. 27684496 2017