OBO ID: DOID:0050453
Term Name: lissencephaly Search Ontology:
Synonyms:
Definition: A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation. (2)
References:
  • GARD:12291
  • ICD10CM:Q04.3
  • MESH:D054082
  • NCI:C103921
  • OMIM:PS607432
  • ORDO:102009
  • SNOMEDCT_US_2023_03_01:204036008
  • SNOMEDCT_US_2023_03_01:23024003
  • UMLS_CUI:C0266463
  • UMLS_CUI:C0266483
Ontology: Human Disease   ( DOID:0050453 )
Relationships
is a type of:
has subtype:
OTHER lissencephaly PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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