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Details
Link-It Detail - Disease - Delirium
Debug Stats
  • ### Total Build Time: 178 ms 25.291 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 314 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 344 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=13 ms Completed: 13 ms rowSize= 201 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 1,012 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 5.399 KB
  • CONCEPT_RELATIONSHIPS gt=131 ms Completed: 131 ms rowSize= 13.322 KB
  • CONCEPT_GENES gt=16 ms Completed: 15 ms rowSize= 3.564 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.143 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Disease (1)
Delirium C0011206
Definition (1)
A disorder characterized by the acute and sudden development of confusion, illusions, movement changes, inattentiveness, agitation, and hallucinations. Usually, it is a reversible condition.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (2)
img Delirium, Dementia, Amnestic, Cognitive Disorders C0029227
img Confusion C0009676
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Delirium, Dementia, Amnestic, Cognitive Disorders C00292273img Delirium, Dementia, Amnestic, Cognitive Disorders C0029227
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Confusion C0009676
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Confusion C0009676
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250414img Confusion C0009676
Relationships (89)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 25
diso_​to_​diso : 58
diso_​to_​phen : 1
diso_​to_​phys : 3


Relationships:
none : 53
isa : 19
mapped_​to : 7
may_​treat : 6
related_​to : 3
replaces : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO175img COMPL POSTOP C0032787
DISO_to_DISO156img chemically induced C0007994
DISO_to_DISO113img Complication Aspects C1171258
DISO_to_DISO112img chemically induced C0007994
DISO_to_DISO92img Cognition Disorders C0009241
DISO_to_DISO88img Dementia C0497327
DISO_to_CHEM77img ANTIPSYCHOTICS C0040615
DISO_to_DISO68img COMPL POSTOP C0032787
DISO_to_CHEM60img ANTIPSYCHOTICS C0040615
DISO_to_DISO53img Complication Aspects C1171258
DISO_to_DISO51img Critical Illness C0010340
DISO_to_ANAT42img In Blood C0005768
DISO_to_DISO41img Dementia C0497327
DISO_to_DISO35img Cognition Disorders C0009241
DISO_to_DISO35img Neoplasms C0027651
DISO_to_DISO34img Hip Fractures C0019557
DISO_to_DISO32img Depression C0011570
DISO_to_CHEM30img Hypnotics and Sedatives C0020592
DISO_to_DISO30img Confusion C0009676
DISO_to_DISO29img Neoplasms C0027651
DISO_to_DISO26img Agitation C0085631
DISO_to_DISO25img Cerebrovascular accident C0038454
DISO_to_DISO23img Hip Fractures C0019557
DISO_to_CHEM21img Haloperidol C0018546
DISO_to_CHEM20img Analgesics, Opioid C0002772
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
img GENERIF, Score=660, Pubmed Id: 17728664, UMLKSK CUI: C0011206
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
img OMIM, Score=1000, UMLKSK CUI: C0011206
HumanSOAT16646sterol O-acyltransferase 1
img GENERIF, Score=827, Pubmed Id: 17593314, UMLKSK CUI: C0011206
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011206Delirium0self