lissencephaly
true
ORDO:102009
SNOMEDCT_US_2018_03_01:23024003
UMLS_CUI:C0266463
UMLS_CUI:C0266483
MESH:D054082
OMIM:615191
ICD10CM:Q04.8
NCI:C103921
ICD10CM:Q04.3
OMIM:300215
disease_ontology
OMIM:614019
DOID:0050453
OMIM:611603
OMIM:607432
Xref MGI.
OMIM mapping confirmed by DO. [SN].
GARD:12291
Lissencephaly is a malformation of cortical development, where there is deficient gyration (folding) in the cerebral cortex, resulting in absent gyri (agyria) and/or broad simple gyri (pachygyria).
OMIM:300067
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.
Malformations of Cortical Development