MB4CICD-11 MMS 2026-01
Gerstmann syndrome
Description
Gerstmann syndrome is a very rare neurological disorder characterised 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.
Index terms
- Gerstmann syndrome
Excludes
8E02.1– Gerstmann-Straussler-Scheinker syndrome
Exclusions from above levels
Sibling codes
MB40– Sensation disturbanceMB41– Disturbances of smell or tasteMB42– PhonophobiaMB43– DyssomniaMB44– Abnormalities of gait or mobilityMB45– Lack of coordinationMB46– Abnormal involuntary movementsMB47– Abnormality of tonus or reflexMB48– Dizziness or giddinessMB49– AuraMB4A– ApraxiaMB4B– Symbolic dysfunctionsMB4D– Headache, not elsewhere classifiedMB60– SleeptalkingMB6Y– Other specified symptoms or signs involving the nervous system
Foundation entity
Gerstmann syndrome – http://id.who.int/icd/entity/1121787098
Part of: 21: Symptoms, signs or clinical findings, not elsewhere classified