HNF4A, hepatocyte nuclear factor 4 alpha, 3172

N. diseases: 340; N. variants: 74
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Diabetes Mellitus, Non-Insulin-Dependent
1.000 Biomarker disease GENOMICS_ENGLAND
Diabetes Mellitus, Non-Insulin-Dependent
1.000 CausalMutation disease CLINVAR
Diabetes Mellitus, Non-Insulin-Dependent
1.000 Biomarker disease GENOMICS_ENGLAND
Diabetes Mellitus, Non-Insulin-Dependent
1.000 Biomarker disease HPO
Maturity-Onset Diabetes of the Young, Type 1
1.000 Biomarker disease GENOMICS_ENGLAND
Maturity-Onset Diabetes of the Young, Type 1
1.000 Biomarker disease GENOMICS_ENGLAND
Maturity-Onset Diabetes of the Young, Type 1
1.000 Biomarker disease GENOMICS_ENGLAND
Maturity-Onset Diabetes of the Young, Type 1
1.000 Biomarker disease MGD
Maturity onset diabetes mellitus in young
0.700 Biomarker disease GENOMICS_ENGLAND
Maturity onset diabetes mellitus in young
0.700 Biomarker disease HPO
Maturity onset diabetes mellitus in young
0.700 Biomarker disease GENOMICS_ENGLAND
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG
0.700 Biomarker disease CTD_human
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes
0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes
0.600 Biomarker disease GENOMICS_ENGLAND
Hyperinsulinism due to HNF4A deficiency
0.400 CausalMutation disease CLINVAR
Hyperinsulinism due to HNF4A deficiency
0.400 GeneticVariation disease CLINVAR
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.200 Biomarker group HPO
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.200 Biomarker disease HPO
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.200 CausalMutation disease CLINVAR
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.200 GeneticVariation disease CLINVAR
CUI: C1864903
Disease: Hyperinsulinemic hypoglycemia
Hyperinsulinemic hypoglycemia
0.200 Biomarker disease HPO
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism
0.200 CausalMutation disease CLINVAR
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism
0.200 Biomarker disease HPO
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
0.180 Biomarker disease HPO
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis
0.180 Biomarker disease HPO