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Metadata
ID	DOID:0112236
Name	lissencephaly 6
Definition	A microlissencephaly characterized by severe microcephaly, developmental delay, lissencephaly, pachygyria, and hypoplasia of the corpus callosum that has_material_basis_in homozygous or compound heterozygous mutation in the KATNB1 gene on chromosome 16q21. https://pubmed.ncbi.nlm.nih.gov/25521378/, https://pubmed.ncbi.nlm.nih.gov/25521379/
Xrefs	MIM:616212
Synonyms	LIS6 [EXACT]
Parent Relationships	is_a microlissencephaly is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance