Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the HCN1 gene.
Comprehensive, easy-to-understand information about this condition
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developmental and epileptic encephalopathy, 39
MONDO:0013056
developmental and epileptic encephalopathy, 12
MONDO:0013389
developmental and epileptic encephalopathy, 13
MONDO:0013801
developmental and epileptic encephalopathy, 16
MONDO:0014133
developmental and epileptic encephalopathy, 21
MONDO:0014360
developmental and epileptic encephalopathy, 25
MONDO:0014392