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Details
Link-It Detail - Disease - Gerstmann Syndrome
Debug Stats
  • ### Total Build Time: 62 ms 8.864 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 545 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
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  • CONCEPT_RELATIONSHIPS gt=12 ms Completed: 12 ms rowSize= 1.993 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=11 ms Completed: 11 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Gerstmann Syndrome C0017494
Definition (1)
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)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Agnosia C0001816
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neurologic Manifestations C00278546img Agnosia C0001816
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370887img Agnosia C0001816
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250415img Agnosia C0001816
Relationships (3)

Relation Types:
diso_​to_​diso : 3


Relationships:
none : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO3img Cognition Disorders C0009241
DISO_to_DISO2img COMPL POSTOP C0032787
DISO_to_DISOpermuted_term_ofimg ANGULAR GYRUS SYNDROME C0017494
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0017494Gerstmann Syndrome0self