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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)
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last database update
MGI 6.22
The Jackson Laboratory