Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 805
Gene Symbol: CALM2
CALM2
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.400 GermlineCausalMutation ORPHANET Novel calmodulin mutations associated with congenital arrhythmia susceptibility. 24917665

2014
Entrez Id: 805
Gene Symbol: CALM2
CALM2
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.400 GermlineCausalMutation ORPHANET Calmodulin mutations associated with recurrent cardiac arrest in infants. 23388215

2013