Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1859
Gene Symbol: DYRK1A
DYRK1A
CUI: C0036572
Disease: Seizures
Seizures 		0.120 GeneticVariation CLINVAR DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. 25944381

2015
Entrez Id: 1859
Gene Symbol: DYRK1A
DYRK1A
CUI: C0036572
Disease: Seizures
Seizures 		0.120 CausalMutation CLINVAR DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. 25944381

2015