Additional Disease Briefs

lissencephaly due to LIS1 mutation

Also known as: LIS1, PAFAH1B1-related lissencephaly, lissencephaly 1, lissencephaly sequence, isolated, lissencephaly, classic, subcortical band heterotopia, subcortical laminar heterotopia

lissencephaly due to TUBA1A mutation

Also known as: LIS3, lissencephaly 3

lissencephaly type 1 due to doublecortin gene mutation

Also known as: Dc syndrome, Double cortex syndrome, LISX, LISX1, X-linked lissencephaly, X-linked lissencephaly type 1, XLIS, Xlis, lissencephaly X-linked, lissencephaly and agenesis of corpus callosum, lissencephaly type 1 due to doublecortin gene mutation, lissencephaly, X-linked, lissencephaly, X-linked, 1, lissencephaly, X-linked, type 1, subcortical band heterotopia, X-linked, subcortical laminal heterotopia, X-linked, subcortical laminar heterotopia, X-linked, subcortical laminar heterotopia, X-linked,

lissencephaly type 3

lissencephaly type 3-familial fetal akinesia sequence syndrome

lissencephaly type 3-metacarpal bone dysplasia syndrome

Also known as: lissencephaly type 3 and bone dysplasia, lissencephaly type III and bone dysplasia

lissencephaly with cerebellar hypoplasia

Also known as: LCH

lissencephaly with cerebellar hypoplasia type A

lissencephaly with cerebellar hypoplasia type B