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Details
Link-It Detail - Disease - Aphasia
Debug Stats
  • ### Total Build Time: 135 ms 28.396 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 424 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=8 ms Completed: 8 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.827 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 5.378 KB
  • CONCEPT_RELATIONSHIPS gt=101 ms Completed: 101 ms rowSize= 13.144 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 5.424 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Aphasia C0003537
Definition (1)
cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form; caused by diseases which affect the language areas of the dominant hemisphere; general categories include receptive, expressive, and mixed forms of aphasia.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Speech Disorders C0037822
Children (4)
img Aphasia, Primary Progressive C0282513
img Aphasia, Conduction C0234471
img Aphasia, Broca C0003550
img Aphasia, Wernicke C1510456
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Mental Disorders Diagnosed in Childhood C05250406img Speech Disorders C0037822
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370888img Speech Disorders C0037822
img Nervous System Diseases C0027765img Neurologic Manifestations C00278547img Speech Disorders C0037822
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250416img Speech Disorders C0037822
Relationships (89)

Relation Types:
diso_​to_​anat : 7
diso_​to_​diso : 73
diso_​to_​phys : 9


Relationships:
none : 31
classifies : 2
isa : 27
mapped_​to : 25
permuted_​term_​of : 1
related_​to : 2
use : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO164img Cerebrovascular accident C0038454
DISO_to_DISO73img Cerebrovascular accident C0038454
DISO_to_ANAT69img Brain C0006104
DISO_to_DISO60img Complication Aspects C1171258
DISO_to_ANAT44img Brain C0006104
DISO_to_PHYS37img Functional Laterality C1720777
DISO_to_PHYS36img Speech Perception C0037826
DISO_to_PHYS33img Speech C0037817
DISO_to_DISO28img Dementia C0497327
DISO_to_PHYS28img Perception, Speech C0037826
DISO_to_DISO27img Complication Aspects C1171258
DISO_to_PHYS26img Functional Laterality C1720777
DISO_to_ANAT22img Temporal Lobe C0039485
DISO_to_DISO22img Recovery of Function C0599766
DISO_to_PHYS22img Comprehension C0162340
DISO_to_ANAT20img Cerebral cortex C0007776
DISO_to_ANAT20img Frontal Lobe C0016733
DISO_to_DISO20img Memory Disorders C0025261
DISO_to_DISO19img Cognition Disorders C0009241
DISO_to_DISO18img Anomia C0003113
DISO_to_DISO18img Function Recoveries C0599766
DISO_to_DISO16img Cerebral Infarction C0007785
DISO_to_DISO15img Brain Injuries C0270611
DISO_to_DISO15img Cognition Disorders C0009241
DISO_to_PHYS15img Speech C0037817
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C0003537
HumanL1CAM3897L1 cell adhesion molecule
img OMIM, Score=1000, UMLKSK CUI: C0003537
img OMIM, Score=1000, UMLKSK CUI: C0003537
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0003537
HumanGRN2896granulin
INFERRED, Score=800, UMLKSK CUI: C0003537
HumanGJB12705gap junction protein, beta 1, 32kDa
INFERRED, Score=800, UMLKSK CUI: C0003537
HumanATP1A2477ATPase, Na+/K+ transporting, alpha 2 polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0003537
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0003537Aphasia0self