×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
Biomarker
disease
GENOMICS_ENGLAND
Molecular Basis for Autosomal-Dominant Renal Fanconi Syndrome Caused by HNF4A.
31875549
2019
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
CausalMutation
disease
CLINVAR
Hyperinsulinaemic hypoglycaemia, renal Fanconi syndrome and liver disease due to a mutation in the HNF4A gene.
28458902
2017
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
CausalMutation
disease
CLINVAR
Fainting Fanconi syndrome clarified by proxy: a case report.
28693455
2017
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
Biomarker
disease
GENOMICS_ENGLAND
Congenital hyperinsulinism and glycogenosis-like phenotype due to a novel HNF4A mutation.
28242437
2017
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
CausalMutation
disease
CLINVAR
Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical Phenotype.
27245055
2016
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
CausalMutation
disease
CLINVAR
Two patients with HNF4A-related congenital hyperinsulinism and renal tubular dysfunction: A clinical variation which includes transient hepatic dysfunction.
25819479
2015
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
Biomarker
disease
GENOMICS_ENGLAND
Two patients with HNF4A-related congenital hyperinsulinism and renal tubular dysfunction: A clinical variation which includes transient hepatic dysfunction.
25819479
2015
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
GeneticVariation
disease
UNIPROT
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype.
24285859
2014
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
CausalMutation
disease
CLINVAR
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype.
24285859
2014
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
Biomarker
disease
GENOMICS_ENGLAND
Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.
22802087
2012
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
GeneticVariation
disease
UNIPROT
Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.
22802087
2012
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
CausalMutation
disease
CLINVAR
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations.
20164212
2010
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
0.700
Biomarker
disease
CTD_human