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Gerstmann syndrome
Disease Summary
Associated Targets ()
Mondo Description Gerstmann syndrome is a very rare neurological disorder characterized by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe.
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.
DOID:4969
EFO:0007285
GARD:0008660
MESH:D005862
Orphanet:221117
SCTID:36785009
MONDO:0005773
High level summary of knowledge for a disease, including descriptions and datasource references.