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Disease Ontology Browser
Norman-Roberts syndrome (DOID:0060902)
Alliance: disease page
Synonyms: lissencephaly 2; lissencephaly syndrome, Norman-Roberts type
Alt IDs: OMIM:257320, MESH:C537848, ORDO:89844, UMLS_CUI:C0796089
Definition: A lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.


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
02/18/2020
MGI 6.14
The Jackson Laboratory