Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27133
Gene Symbol: KCNH5
KCNH5
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.310 Biomarker GENOMICS_ENGLAND In three children, the de novo variants were in genes with functional roles that are plausibly relevant to epilepsy (KCNH5, CLCN4, and ARHGEF15). 23647072

2013