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Summary Literature (0)
MIM:300067 - LISSENCEPHALY, X-LINKED, 1; LISX1

Xenbase Genes: dcx

Human Disease Resource: MIM

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