Disease: Primary Lesion ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Primary Lesion
CUI: C1402294
Disease: Primary Lesion
0.010 GeneticVariation BEFREE The detection rate of T790M mutations in CSF was 18.1% (2 of 11) in all cases with EGFR-sensitive mutations in the primary lesion. 30452286 2019