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