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DO Term : X-linked lissencephaly 1 [DOID:0112239] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23.

synonyms:
OMIM:300067,
XLIS1,
lissencephaly type 1 due to doublecortin gene mutation,
300067

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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