Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:300067 - LISSENCEPHALY, X-LINKED, 1; LISX1

Xenbase Genes: dcx

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010239 - lissencephaly type 1 due to doublecortin gene mutation
MONDO:0020491 - subcortical band heterotopia

Disease Ontology (DO):
DOID:0050453 - lissencephaly