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Details
Link-It Detail - Disease - Agnosia
Debug Stats
  • ### Total Build Time: 122 ms 22.166 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 534 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 201 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 987 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 4.105 KB
  • CONCEPT_RELATIONSHIPS gt=89 ms Completed: 89 ms rowSize= 12.191 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 2.171 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Agnosia C0001816
Definition (1)
Loss of the ability to comprehend the meaning or recognize the importance of various forms of stimulation that cannot be attributed to impairment of a primary sensory modality. Tactile agnosia is characterized by an inability to perceive the shape and nature of an object by touch alone, despite unimpaired sensation to light touch, position, and other primary sensory modalities.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Perceptual Disorders C0030975
Children (2)
img Prosopagnosia C0234512
img Gerstmann Syndrome C0017494
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Perceptual Disorders C0030975
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Perceptual Disorders C0030975
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250414img Perceptual Disorders C0030975
Relationships (35)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 22
diso_​to_​phys : 11


Relationships:
none : 23
isa : 10
mapped_​to : 1
replaces : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHYS29img Visual Perception C0042830
DISO_to_PHYS23img Awareness C0004448
DISO_to_PHYS23img Pattern Recognition, Visual C0030709
DISO_to_PHYS21img Visual Perception C0042830
DISO_to_ANAT19img Brain C0006104
DISO_to_DISO18img Alzheimer Disease C0002395
DISO_to_DISO18img Perceptual Disorders C0030975
DISO_to_DISO17img Complication Aspects C1171258
DISO_to_DISO17img Hemiplegia C0018991
DISO_to_DISO16img Stroke C0038454
DISO_to_PHYS16img Pattern Recognition, Visual C0030709
DISO_to_PHYS16img Recognition C0524637
DISO_to_DISO14img Alzheimer Disease C0002395
DISO_to_PHYS14img Body Image C0005891
DISO_to_PHYS14img Psychomotor Performance C0033923
DISO_to_DISO13img Cerebrovascular accident C0038454
DISO_to_DISO13img Perceptual Disorders C0030975
DISO_to_PHYS13img Attention C0004268
DISO_to_DISO11img Cognition Disorders C0009241
DISO_to_ANAT10img Cerebral cortex C0007776
DISO_to_DISO10img Cerebral Infarction C0007785
DISO_to_PHYS10img Attention C0004268
DISO_to_PHYS10img Functional Laterality C1720777
DISO_to_DISOisaimg ANOSOGNOSIA C0234507
DISO_to_DISOreplacesimg Agnosia C0001816
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanTREM254209triggering receptor expressed on myeloid cells 2
img OMIM, Score=1000, UMLKSK CUI: C0001816
HumanTYROBP7305TYRO protein tyrosine kinase binding protein
img OMIM, Score=1000, UMLKSK CUI: C0001816
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0001816Agnosia0self