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expandnervous system disorder (MONDO:0005071)
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..expandGerstmann syndrome ()

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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:5773
Name:Gerstmann syndrome
Definition: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.
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Synonyms:aphasia-angular gyrus syndrome; developmental Gerstmann syndrome; Gerstmann Badal syndrome; Gerstmann tetrad; GS
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Reference: MedGen:
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