Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC25A22 gene.
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developmental and epileptic encephalopathy, 9
MONDO:0010246
developmental and epileptic encephalopathy, 8
MONDO:0010375
developmental and epileptic encephalopathy, 2
MONDO:0010396
multiple congenital anomalies-hypotonia-seizures syndrome 2
MONDO:0010466
developmental and epileptic encephalopathy, 36
MONDO:0010472
developmental and epileptic encephalopathy, 1
MONDO:0010632