lissencephaly 8

Summary

DOID:0112233 - lissencephaly 8

Disease Ontology Definition:A lissencephaly characterized by delayed psychomotor development, intellectual disability with poor or absent speech, early-onset refractory seizures, and hypotonia that has_material_basis_in homozygous or compound heterozygous mutation in the TMTC3 gene on chromosome 12q21.32.

Synonyms: LIS8

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tmtc3

MIM:

MIM:617255 - LISSENCEPHALY 8; LIS8

MIM:617255 - LISSENCEPHALY 8; LIS8

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), lissencephaly (is_a)