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Gerstmann Syndrome (CUI C0017494) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0017494

Semantic Type: Mental or Behavioral Dysfunction

MSH Definition: A disorder of cognition characterized by the tetrad of finger agnosia, dysgraphia, DYSCALCULIA, and right-left disorientation. The syndrome may be developmental or acquired. Acquired Gerstmann syndrome is associated with lesions in the dominant (usually left) PARIETAL LOBE which involve the angular gyrus or subjacent white matter. (From Adams et al., Principles of Neurology, 6th ed, p457)

Synonyms & Abbreviations: (see Synonym Details)
ANGULAR GYRUS SYNDROME
Aphasia-angular gyrus syndrome (disorder)
Aphasia-angular gyrus syndrome
de Gerstmann, Syndrome
Finger-Agnosia-Left-Right-Confusion-Acalculia-Agraphias
Finger-Agnosia-Left-Right-Confusion-Acalculia-Agraphia
Gerstmann Badal syndrome
Gerstmann Syndrome [Disease/Finding]
GERSTMANN SYNDROME
Gerstmann tetrad
Gerstmann's syndrome
Gerstmann, Syndrome de
Gerstmann-Badal Syndrome
GS
Syndrome de Gerstmann
Syndrome, Gerstmann-Badal
Syndrome, Gerstmann

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN do not confuse with GERSTMANN-STRAUSSLER SYNDROME, a prion disease MSH
AQL BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000017005 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
CTV3ID XUCdp SNOMEDCT_US
DATE_CREATED 2013-01-09T00:04:00 GARD
DATE_LAST_MODIFIED 2013-01-09T00:04:00 GARD
DC 1 MSH
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DISEASE_IDENTIFIER_ID 3343 GARD
DISEASE_IDENTIFIER_ID 3345 GARD
DISEASE_IDENTIFIER_ID 3346 GARD
DX 20000101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
FX D060705 MSH
HAS_GARD_PAGE true GARD
HN 2000(1966) MSH
IDENTIFIER_TYPE_ID 1 GARD
IS_ACTIVE true GARD
IS_RARE true GARD
IS_SPANISH false GARD
MDA 19990101 MSH
MESH_DEFINITION A disorder of cognition characterized by the tetrad of finger agnosia, dysgraphia, DYSCALCULIA, and right-left disorientation. The syndrome may be developmental or acquired. Acquired Gerstmann syndrome is associated with lesions in the dominant (usually left) PARIETAL LOBE which involve the angular gyrus or subjacent white matter. (From Adams et al., Principles of Neurology, 6th ed, p457) NDFRT
MESH_DUI D005862 NDFRT
MESH_NAME Gerstmann Syndrome NDFRT
MESH_UI M0009211 NDFRT
MMR 20110624 MSH
MN C10.597.606.762.100.300 MSH
MN C23.888.592.604.764.100.300 MSH
MN F01.700.750.100.300 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000001328 NDFRT
PM 2000; see Gerstmann's Syndrome 1966-1999 MSH
PRIMARY_PATH 10048608$10011168$10029305$10029205$Gerstmann's syndrome$Cortical dysfunction NEC$Neurological disorders NEC$Nervous system disorders MDR
PRIMARY_SOC 10029205 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 20.0 MDR
PT_IN_VERSION 20.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/8660/gerstmann-syndrome/resources/1 GARD
RXAUI 3160710 RXNORM
RXAUI 3165320 RXNORM
RXAUI 3165321 RXNORM
RXAUI 3165324 RXNORM
RXAUI 3605844 RXNORM
RXAUI 3606352 RXNORM
RXCUI 1026723 RXNORM
SNOMED_CID 36785009 NDFRT
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS F81.3 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~F81.3 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS R48.8 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~R48.8 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUCdp SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T017737 MSH
TERMUI T365785 MSH
TERMUI T372725 MSH
TERMUI T756693 MSH
TERMUI T769361 MSH
TH NLM (1966) MSH
TH NLM (2000) MSH
TH NLM (2011) MSH
TH ORD (2010) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0017494

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