Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET	C4310743	VAC14	Causal Pathogenic evidence from ClinVar	19037259, 27292112	ClinVar
STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET	C4310743	VAC14-AS1	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	-	-
STRIATONIGRAL DEGENERATION, INFANTILE (disorder)	C0795996	ADAR	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	24262145	-
		ATP6	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	-	-
		IL4I1	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	-	-
		NUP62	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	12374138, 14718703, 16786527, 27604308	-
Striatonigral Degeneration, Infantile, Mitochondrial	C1839022	ATP6	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	7668837	-
Striatonigral Degeneration	C0270733	COQ2	Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations	23758206	-

Striatonigral degeneration