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lissencephaly 4
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any lissencephaly in which the cause of the disease is a mutation in the NDE1 gene.
Uniprot Description A neurodevelopmental disorder characterized by lissencephaly, severe brain atrophy, extreme microcephaly, and profound mental retardation.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:614019
UMLS:C3151461
MONDO:0013527
High level summary of knowledge for a disease, including descriptions and datasource references.