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Details
Link-It Detail - Disease - Amnesia
Debug Stats
  • ### Total Build Time: 185 ms 35.887 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 222 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=0 Completed: 0 ms rowSize= 1,019 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 1.838 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 5.420 KB
  • CONCEPT_RELATIONSHIPS gt=146 ms Completed: 146 ms rowSize= 13.498 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 12.249 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Amnesia C0002622
Definition (1)
A disorder characterized by systematic and extensive loss of memory.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (2)
img Memory Disorders C0025261
img Delirium, Dementia, Amnestic, Cognitive Disorders C0029227
Children (4)
img Amnesia, Anterograde C0233795
img Amnesia, Retrograde C0002624
img Amnesia, Transient Global C0338591
img Alcohol Amnestic Disorder C0001940
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Memory Disorders C0025261
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Memory Disorders C0025261
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250414img Memory Disorders C0025261
img Mental Disorders C0004936img Delirium, Dementia, Amnestic, Cognitive Disorders C00292273img Delirium, Dementia, Amnestic, Cognitive Disorders C0029227
Relationships (82)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 17
diso_​to_​diso : 35
diso_​to_​phen : 1
diso_​to_​phys : 19


Relationships:
none : 56
induces : 11
isa : 9
mapped_​to : 3
parent_​is_​cdrh : 1
permuted_​term_​of : 1
used_​for : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO198img Cognition Disorders C0009241
DISO_to_DISO107img chemically induced C0007994
DISO_to_DISO91img Alzheimer Disease C0002395
DISO_to_DISO91img Complication Aspects C1171258
DISO_to_PHYS84img Memory C0025260
DISO_to_DISO80img chemically induced C0007994
DISO_to_ANAT77img Hippocampus C0019564
DISO_to_ANAT72img Brain C0006104
DISO_to_PHYS62img Memory C0025260
DISO_to_PHYS61img Mental Recall C0034770
DISO_to_DISO43img Cognition Disorders C0009241
DISO_to_DISO42img Alzheimer Disease C0002395
DISO_to_PHYS40img Recognition C0524637
DISO_to_PHYS35img Mental Recall C0034770
DISO_to_DISO34img Mild cognitive disorder C1270972
DISO_to_ANAT31img Hippocampus C0019564
DISO_to_DISO31img Brain Injuries C0270611
DISO_to_ANAT30img Temporal Lobe C0039485
DISO_to_DISO21img Complication Aspects C1171258
DISO_to_PHEN21img genetic aspects C0017399
DISO_to_ANAT20img Brain C0006104
DISO_to_ANAT20img Temporal Lobe C0039485
DISO_to_DISO19img Dementia C0497327
DISO_to_PHYS16img Learning C0023185
DISO_to_PHYS16img Recognition C0524637
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanCHMP2B25978charged multivesicular body protein 2B
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
INFERRED, Score=800, UMLKSK CUI: C0002622
HumanEIF2B58893eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanEIF2B28892eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanEIF2B38891eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanEIF2B48890eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanTKT7086transketolase
INFERRED, Score=800, UMLKSK CUI: C0002622
HumanSLC6A46532solute carrier family 6 (neurotransmitter transporter), member 4
INFERRED, Score=800, UMLKSK CUI: C0002622
HumanPSEN15663presenilin 1
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanPRKCG5582protein kinase C, gamma
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanGRN2896granulin
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanFGF142259fibroblast growth factor 14
img OMIM, Score=1000, UMLKSK CUI: C0002622
HumanEIF2B11967eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
img OMIM, Score=1000, UMLKSK CUI: C0002622
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002622Amnesia0self