|
DOID:0050453 - lissencephaly
Disease Ontology Definition:A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.
Synonyms:
Xenbase Genes
:
arx,
reln,
dcx,
katnb1,
pafah1b1,
nde1,
cdk5,
lamb1,
tuba1cl.3,
tmtc3,
tuba1a
| MONDO:0018838 - lissencephaly spectrum disorders |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital nervous system abnormality (is_a)