DISEASES

Disease-gene associations mined from literature

Human genes for lissencephaly

Lissencephaly [DOID:0050453]

A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.

Synonyms:  lissencephaly,  DOID:0050453

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8