OBO ID: DOID:0112238
Term Name: X-linked lissencephaly 2 Search Ontology:
Synonyms:
  • X-linked lissencephaly with abnormal genitalia
  • X-linked lissencephaly with ambiguous genitalia
  • X-linked lissencephaly-corpus callosum agenesis-genital anomalies syndrome
  • XLAG
  • XLAG (X-linked lissencephaly with abnormal genitalia) syndrome
  • XLIS2
Definition: A lissencephaly characterized by structural brain anomalies, early-onset intractable seizures, severe psychomotor retardation, and ambiguous genitalia that has_material_basis_in mutation in ARX on chromosome Xp21.3. (2)
References:
Ontology: Human Disease   ( DOID:0112238 )
Relationships
is a type of:
OTHER X-linked lissencephaly 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ARX Lissencephaly, X-linked 2 300215
Hydranencephaly with abnormal genitalia 300215
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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