X-linked lissencephaly 1

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Summary

Literature (0)

DOID:0112239 - X-linked lissencephaly 1

Disease Ontology Definition:A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23.

Synonyms: XLIS1, lissencephaly type 1 due to doublecortin gene mutation,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): X-linked monogenic disease (is_a), lissencephaly (is_a)