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rhombencephalosynapsis
Disease Summary
Associated Targets ()
Mondo Description Rhombencephalosynapsis (RS) is a rare malformation of the cerebellum characterised by the association of agenesis (total or partial) of the vermis and fusion of the cerebellar hemispheres.
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:59315
SCTID:442300000
UMLS:C1866130
MONDO:0018946
High level summary of knowledge for a disease, including descriptions and datasource references.