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General Information
ZIRC
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:
Ontology: Human Disease   (DOID:0050453)
OTHER lissencephaly PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ARX Lissencephaly, X-linked 2 300215
Hydranencephaly with abnormal genitalia 300215
LAMB1 Lissencephaly 5 615191
NDE1 Lissencephaly 4 (with microcephaly) 614019
PAFAH1B1 Subcortical laminar heterotopia 607432
Lissencephaly 1 607432
TUBA1A Lissencephaly 3 611603
DCX Lissencephaly, X-linked 300067
Subcortical laminal heterotopia, X-linked 300067
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None