Search Ontology:
Human Disease

X-linked lissencephaly 1

Term ID
DOID:0112239
Synonyms
  • lissencephaly type 1 due to doublecortin gene mutation
  • XLIS1
Definition
A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23. (2)
References
Ontology
Human Disease   ( DOID:0112239 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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