Disease: Intracranial Arterial Diseases ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Intracranial Arterial Diseases
CUI: C0752138
Disease: Intracranial Arterial Diseases
0.010 GeneticVariation BEFREE Genotyping of the p.R4810K missense variant is useful for identifying individuals with an elevated risk for steno-occlusive intracranial arterial diseases in the family members of patients with moyamoya disease. 28506590 2017