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DO Term : lissencephaly 3 [DOID:0112232] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A lissencephaly characterized by brain malformations, microcephaly, developmental delay and epilepsy that has_material_basis_in heterozygous mutation in the TUBA1A gene on chromosome 12q13.12.
  • synonyms:
  • 611603,
  • OMIM:611603,
  • MESH:C566908,
  • LIS3,
  • ORDO:171680
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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