rs797044522, DYRK1A

N. diseases: 9
Disease: Severe speech delay ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Severe speech delay
CUI: C1968537
Disease: Severe speech delay
0.700 CausalMutation CLINVAR DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. 25944381 2015