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Disease Ontology Browser
lissencephaly 3 (DOID:0112232)
Alliance: disease page
Synonyms: 'LIS3'
Alt IDs: OMIM:611603, ORDO:171680
Definition: A lissencephaly characterized by brain malformations, microcephaly, developmental delay and epilepsy that has_material_basis_in heterozygous mutation in TUBA1A on chromosome 12q13.12.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/16/2021
MGI 6.17
The Jackson Laboratory