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DO Term : lissencephaly 10 [DOID:0112229] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A lissencephaly characterized by variably delayed development, mildly to moderately impaired intellectual development and language delay, seizures, brain features consistent with neuronal migration defects that has_material_basis_in heterozygous mutation in the CEP85L gene on chromosome 6q22.31.
  • synonyms:
  • 618873,
  • OMIM:618873,
  • LIS10
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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