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DO Term : lissencephaly 4 [DOID:0112235] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A microlissencephaly characterized by lissencephaly, severe brain atrophy, extreme microcephaly, and profound intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the NDE1 gene on chromosome 16p13.11.
  • synonyms:
  • OMIM:614019,
  • lissencephaly 4 with microcephaly,
  • LIS4,
  • 614019
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Disease

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Diseases --> Mouse genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents