Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease GENOMICS_ENGLAND Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey. 27181376 2016
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease CLINGEN Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation. 23273570 2013
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease CLINGEN Diagnosis of a patient with a kinetic variant of medium and short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency by newborn screening. 22579592 2012
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease CLINGEN 3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations. 23430856 2012
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease CLINGEN Role of medium- and short-chain L-3-hydroxyacyl-CoA dehydrogenase in the regulation of body weight and thermogenesis. 21990309 2011
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease CLINGEN Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene. 15870679 2005
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease CLINGEN Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion. 11489939 2001
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 GeneticVariation disease UNIPROT
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 GermlineCausalMutation disease ORPHANET
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease CTD_human
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 GeneticVariation disease CLINVAR
Entrez Id: 3033
Gene Symbol: HADH
HADH
0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 3078
Gene Symbol: CFHR1
CFHR1
0.010 Biomarker disease BEFREE Laboratory analyses performed showed that in total 78 cases had findings consistent with complement-mediated aHUS: 24 cases indicated presence of CFH-specific antibodies whereof five cases had isolated low C3 titres and six cases had deficiency of CFHR1. 27175932 2017
Entrez Id: 1200
Gene Symbol: TPP1
TPP1
0.010 AlteredExpression disease BEFREE All probands had deficiency of tripeptidyl-peptidase I (TPP1) activity and, at the EM level, curvilinear profiles. 11073228 2000
Entrez Id: 3502
Gene Symbol: IGHG3
IGHG3
0.010 AlteredExpression disease BEFREE In order to get to clues about T-cell independent versus T-cell dependent immune mechanism in ALS, we measured IgG subclasses in 25 ALS-patients: 16 patients had deficiency of T-cell dependent expressed IgG1 or IgG3 or both with essentially normal levels of T-cell independent expressed IgG2 and IgG4. 8475688 1993