OBO ID: DOID:0112239
Term Name: X-linked lissencephaly 1 Search Ontology:
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 X-linked lissencephaly 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DCX Lissencephaly, X-linked
Subcortical laminal heterotopia, X-linked
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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