CALM2, calmodulin 2, 805

N. diseases: 252; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome
0.400 GermlineCausalMutation disease ORPHANET Novel calmodulin mutations associated with congenital arrhythmia susceptibility. 24917665 2014
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome
0.400 GermlineCausalMutation disease ORPHANET Calmodulin mutations associated with recurrent cardiac arrest in infants. 23388215 2013
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome
0.400 GeneticVariation disease CLINVAR