GATA2, GATA binding protein 2, 2624

N. diseases: 229; N. variants: 33
Disease: Emberger Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		0.770 GeneticVariation disease BEFREE Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). 21892158 2011
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		0.770 Biomarker disease GENOMICS_ENGLAND Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). 21892158 2011
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		0.770 Biomarker disease GENOMICS_ENGLAND Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia. 21892162 2011
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		0.770 Biomarker disease GENOMICS_ENGLAND Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases. 20803646 2010
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		0.770 Biomarker disease GENOMICS_ENGLAND
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		0.770 Biomarker disease CTD_human
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		0.770 SusceptibilityMutation disease ORPHANET