TBX19, T-box transcription factor 19, 9095

N. diseases: 35; N. variants: 10
Disease: Neonatal hypoglycemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.110 GeneticVariation disease BEFREE A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation. 29858850 2018
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		0.110 Biomarker disease HPO