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microlissencephaly
Disease Summary
Associated Targets (31)
Tbio
23
Tchem
6
Tdark
2
Mondo Description Microlissencephaly describes a heterogenous group of a rare cortical malformations characterized by lissencephaly in combination with severe congenital microcephaly, presenting with spasticity, severe developmental delay, and seizures and with survival varying from days to years.
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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:1083
UMLS:C1956147
MONDO:0015204
High level summary of knowledge for a disease, including descriptions and datasource references.