|
epileptic encephalopathy, early infantile, type 7
|
13387 |
|
|
KCNQ2-related neonatal epileptic encephalopathy
|
13387 |
|
|
early infantile epileptic encephalopathy 12
|
13389 |
|
|
early infantile epileptic encephalopathy caused by mutation in PLCB1
|
13389 |
|
|
early infantile epileptic encephalopathy caused by mutation in SCN2A
|
13388 |
|
|
developmental and epileptic encephalopathy, 11
|
13388 |
|
|
developmental and epileptic encephalopathy, 12
|
13389 |
|
|
developmental and epileptic encephalopathy, 7
|
13387 |
|
|
recurrent vertigo, episodic
|
D020338 |
|
|
recurrent vertigos, episodic
|
D020338 |
|
|
primary ovarian failure arising through autoimmunity
|
44338 |
|
|
SCN2A early infantile epileptic encephalopathy
|
13388 |
|
|
epilepsy, idiopathic generalized, susceptibility to, 4
|
12338 |
|
