Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Disease - Memory Disorders
Debug Stats
  • ### Total Build Time: 38 ms 32.066 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 251 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=3 ms Completed: 3 ms rowSize= 566 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 981 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.135 KB
  • CONCEPT_RELATIONSHIPS gt=23 ms Completed: 23 ms rowSize= 13.400 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 11.079 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Memory Disorders C0025261
Definition (1)
disturbances in registering, retaining, or recalling a mental impression; e.g., amnesia or fugue.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Neurobehavioral Manifestations C0525041
Children (2)
img Korsakoff Syndrome C0349464
img Amnesia C0002622
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Neurobehavioral Manifestations C0525041
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Neurobehavioral Manifestations C0525041
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250413img Neurobehavioral Manifestations C0525041
Relationships (184)

Relation Types:
diso_​to_​anat : 21
diso_​to_​chem : 35
diso_​to_​diso : 70
diso_​to_​phen : 2
diso_​to_​phys : 56


Relationships:
none : 180
mapped_​to : 1
permuted_​term_​of : 1
use : 2
Page Size
Current 25
  Page 1 of 8
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO481img Cognition Disorders C0009241
DISO_to_DISO450img chemically induced C0007994
DISO_to_PHYS374img Immediate Memories C0025265
DISO_to_DISO359img Alzheimer Disease C0002395
DISO_to_ANAT347img Hippocampus C0019564
DISO_to_PHYS346img Memory C0025260
DISO_to_DISO326img chemically induced C0007994
DISO_to_DISO314img Cognition Disorders C0009241
DISO_to_PHYS269img Aging C0001811
DISO_to_ANAT258img Hippocampus C0019564
DISO_to_PHEN246img genetic aspects C0017399
DISO_to_ANAT244img Brain C0006104
DISO_to_PHYS236img Mental Recall C0034770
DISO_to_DISO218img Alzheimer Disease C0002395
DISO_to_DISO210img Complication Aspects C1171258
DISO_to_PHYS202img Memory C0025260
DISO_to_DISO193img Schizophrenia C0036341
DISO_to_PHYS192img Aging C0001811
DISO_to_DISO161img Academic skill disorder C0023186
DISO_to_DISO149img Schizophrenia C0036341
DISO_to_DISO144img Dementia C0497327
DISO_to_PHYS143img Recognition C0524637
DISO_to_DISO141img Brain Injuries C0270611
DISO_to_PHEN135img genetic aspects C0017399
DISO_to_ANAT130img Brain C0006104
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanCHMP2B25978charged multivesicular body protein 2B
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanEIF2B58893eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanEIF2B28892eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanEIF2B38891eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanEIF2B48890eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanTP537157tumor protein p53
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanTKT7086transketolase
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanSLC6A46532solute carrier family 6 (neurotransmitter transporter), member 4
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanPSEN15663presenilin 1
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanPRNP5621prion protein
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanPRKCG5582protein kinase C, gamma
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanHTR2A33565-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanHLA-DQB13119
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanGRN2896granulin
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanFGF142259fibroblast growth factor 14
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanEIF2B11967eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
INFERRED, Score=800, UMLKSK CUI: C0025261
HumanAPOE348apolipoprotein E
INFERRED, Score=800, UMLKSK CUI: C0025261
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0025261Memory Disorders0self