HNF1A, HNF1 homeobox A, 6927

N. diseases: 292; N. variants: 105
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.050 GeneticVariation disease BEFREE Different phenotypes of HNF1ß deletion mutants in familial multicystic dysplastic kidneys. 23725647 2013
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.050 GeneticVariation disease BEFREE The appearance of fasting hyperglycaemia following rhGH treatment in children with renal cystic hypodysplasia suggests that investigation of the HNF1 beta gene is warranted, even when familial history is negative for diabetes. 20543213 2010
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.050 GeneticVariation disease BEFREE Analysis of a non-functional HNF-1alpha (TCF1) mutation in Japanese subjects with familial type 1 diabetes. 11668618 2001
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.050 Biomarker disease BEFREE Molecular scanning analysis of hepatocyte nuclear factor 1alpha (TCF1) gene in typical familial type 2 diabetes in African Americans. 10690959 2000
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.050 Biomarker disease BEFREE To evaluate the role of HNF1 alpha in the more common familial type 2 diabetes, we studied 62 families of Northern European origin by linkage analysis and molecular screening. 9626139 1998