Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 513
Gene Symbol: ATP5F1D
ATP5F1D
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. 29478781

2018
Entrez Id: 55252
Gene Symbol: ASXL2
ASXL2
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR

Entrez Id: 2719
Gene Symbol: GPC3
GPC3
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 GeneticVariation CLINVAR

Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR

Entrez Id: 2581
Gene Symbol: GALC
GALC
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 GeneticVariation CLINVAR

Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR

Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR

Entrez Id: 51322
Gene Symbol: WAC
WAC
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR

Entrez Id: 9091
Gene Symbol: PIGQ
PIGQ
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 GeneticVariation CLINVAR

Entrez Id: 51371
Gene Symbol: POMP
POMP
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR

Entrez Id: 64324
Gene Symbol: NSD1
NSD1
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.100 CausalMutation CLINVAR