|
mitochondrial complex IV deficiency, nuclear-type
|
33885 |
|
|
ampulla of Vater clear cell adenocarcinoma
|
3388 |
|
|
hepatopancreatic ampulla clear cell adenocarcinoma
|
3388 |
|
|
epileptic encephalopathy, early infantile, 11
|
13388 |
|
|
epileptic encephalopathy, early infantile, 11; EIEE11
|
http://purl.obolibrary.org/obo/MONDO_0013388 |
|
|
epileptic encephalopathy, early infantile, type 11
|
13388 |
|
|
early infantile epileptic encephalopathy caused by mutation in SCN2A
|
13388 |
|
|
developmental and epileptic encephalopathy, 11
|
13388 |
|
|
SCN2A early infantile epileptic encephalopathy
|
13388 |
|
|
ampulla of vater clear cell adenocarcinoma
|
3388 |
|
