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DOID:1826 - epilepsy
Disease Ontology Definition:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.
Synonyms: epilepsy syndrome, epileptic syndrome
Xenbase Genes
:
atp6v1a,
slc12a5,
arx,
prickle1,
cux2,
lmnb2,
aldh7a1,
kcnq3,
clcn2,
chrnb2,
nprl2,
gal,
gnao1,
ntrk2,
st3gal3,
| MONDO:0005027 - mucosa of frontal sinus |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
brain disease (is_a)