Gene: MEIS2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2 		0.110 Biomarker disease BEFREE By reviewing this patient and previous patients with MEIS2 point mutations, we found that feeding difficulty with gastro-esophageal reflux appears to be one of the core clinical features of MEIS2 haploinsufficiency, in addition to intellectual disability, cleft palate and cardiac septal defect. 27225850 2016
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2 		0.110 Biomarker disease HPO