Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
FEINGOLD SYNDROME 1	C4551774	MYCN	Causal Pathogenic evidence from ClinVar	15821734, 16906565, 18470948	ClinVar
FEINGOLD SYNDROME 1	C4551774	MYCNOS	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	-	-
Feingold syndrome type 1	391641	MYCN	Causal Pathogenic evidence from ClinVar	-	ClinVar
Oculodigitoesophagoduodenal syndrome	C0796068	MYCN	Causal Pathogenic evidence from ClinVar	15821734, 18470948, 19852433, 21532573	ClinVar
Oculodigitoesophagoduodenal syndrome	C0796068	MIR17HG	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	19344873, 26360630	-
FEINGOLD SYNDROME 2	C3280489	MIR17HG	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	19344873, 21892160, 26360630	-
Feingold syndrome type 2	391646	MIR17HG	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	-	-

Feingold syndrome