About   Help   FAQ
Disease Ontology Browser
lissencephaly (DOID:0050453)
Alliance: disease page
Alt IDs: ICD10CM:Q04.3, MESH:D054082, NCI:C103921, OMIM:PS607432, ORDO:102009, UMLS_CUI:C0266463, UMLS_CUI:C0266483
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.

Disease References using Mouse Models (9)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory