Gene: KMT2D ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8085
Gene Symbol: KMT2D
KMT2D 		0.110 GeneticVariation group BEFREE In conclusion, a CHD is detected in 70% of patients with KMT2D (MLL2) pathogenic variants, most commonly left-sided obstructive lesions, including multiple left-sided obstructions similar to those observed in the spectrum of the Shone complex, and septal defects. 28884922 2017
Entrez Id: 8085
Gene Symbol: KMT2D
KMT2D 		0.110 Biomarker group HPO