KMT5A, lysine methyltransferase 5A, 387893

N. diseases: 49; N. variants: 4
Disease: Anemia, severe ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0238644
Disease: Anemia, severe
Anemia, severe 		0.010 GeneticVariation disease BEFREE Erythroid Setd8 deletion results in embryonic lethality from severe anemia due to impaired erythroblast survival and proliferation. 29186677 2017