Preferred Name | Gerstmann syndrome | |
Synonyms |
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Definitions |
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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ID |
http://www.orpha.net/ORDO/Orphanet_221117 |
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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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definition_citation |
Orphanet |
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expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=221117 |
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hasDbXref |
ICD-10:F81.2 MedDRA:10048608 ICD-11:MB4C UMLS:C0017494 MeSH:D005862 |
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label |
Gerstmann syndrome |
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notation |
ORPHA:221117 |
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part_of | ||
prefixIRI |
ORDO:Orphanet_221117 |
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prefLabel |
Gerstmann syndrome |
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treeView | ||
subClassOf |