CCRL2, C-C motif chemokine receptor like 2, 9034

N. diseases: 59; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0424101
Disease: Inattention
Inattention
0.010 GeneticVariation phenotype BEFREE The domain of inattention and omission errors was related to occupational/vocational therapy engagement as well as a higher risk of present and future violence as measured by the HCR-20. 31133891 2019