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Disease Ontology Browser
X-linked lissencephaly 1 (DOID:0112239)
Alliance: disease page
Synonyms: lissencephaly type 1 due to doublecortin gene mutation; XLIS1
Alt IDs: OMIM:300067
Definition: A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23.

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory