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Disease association ontology term - MONDO:0018838 - lissencephaly spectrum disorders

Term summary

ID
MONDO:0018838
Name
lissencephaly spectrum disorders
Ontology or CV name
Disease association
Definition
The term lissencephaly covers a group of rare malformations sharing the common feature of anomalies in the appearance of brain convolutions (characterized by simplification or absence of folding) associated with abnormal organization of the cortical layers as a result of neuronal migration defects during embryogenesis.

Parents

Annotation

Disease association

MONDO:0018838 - lissencephaly spectrum disorders

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MONDO:0013812 - Baraitser-winter syndrome 2

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MONDO:0014596 - lissencephaly 7 with cerebellar hypoplasia

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MONDO:0012703 - lissencephaly due to TUBA1A mutation

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MONDO:0009736 - Neu-Laxova syndrome 1

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MONDO:0014466 - Neu-Laxova syndrome 2

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MONDO:0014296 - Warburg micro syndrome 4

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