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Details
Link-It Detail - Disease - Confusion
Debug Stats
  • ### Total Build Time: 49 ms 34.422 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 235 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=0 Completed: 0 ms rowSize= 253 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=2 ms Completed: 2 ms rowSize= 546 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.135 KB
  • CONCEPT_RELATIONSHIPS gt=26 ms Completed: 26 ms rowSize= 12.504 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 14.741 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Confusion C0009676
Definition (1)
A mental state characterized by a lack of clear and orderly thought and behavior.
Semantic Types (2)
Sign or Symptom (T184)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Neurobehavioral Manifestations C0525041
Children (1)
img Delirium C0011206
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 (50)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 1
diso_​to_​diso : 42
diso_​to_​phys : 4


Relationships:
none : 41
isa : 3
mapped_​to : 4
parent_​is_​cdrh : 1
replaces : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO39img chemically induced C0007994
DISO_to_DISO34img chemically induced C0007994
DISO_to_DISO30img Delirium C0011206
DISO_to_DISO24img COMPL POSTOP C0032787
DISO_to_DISO20img Complication Aspects C1171258
DISO_to_DISO16img Delirium C0011206
DISO_to_DISO16img Dementia C0497327
DISO_to_DISO14img Dementia C0497327
DISO_to_DISO14img Memory Disorders C0025261
DISO_to_DISO12img Alzheimer Disease C0002395
DISO_to_DISO11img Cognition Disorders C0009241
DISO_to_DISO10img Brain Injuries C0270611
DISO_to_DISO10img Cognition Disorders C0009241
DISO_to_DISO10img Headache C0018681
DISO_to_DISO9img Alzheimer Disease C0002395
DISO_to_DISO9img COMPL POSTOP C0032787
DISO_to_DISO9img Seizures C0036572
DISO_to_PHYS9img Orientation C0029266
DISO_to_PHYS9img Space Perception C0037744
DISO_to_DISO8img Complication Aspects C1171258
DISO_to_DISO8img Hallucinations C0018524
DISO_to_DISO8img Psychotic Disorders C0033975
DISO_to_ANAT7img Brain C0006104
DISO_to_ANAT7img In Blood C0005768
DISO_to_DISO7img Brain Neoplasms C0006118
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0009676
HumanNAGS162417N-acetylglutamate synthase
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanAMN81693amnion associated transmembrane protein
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanSLC25A1510166solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
img OMIM, Score=833, UMLKSK CUI: C0009676
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanTKT7086transketolase
img OMIM, Score=1000, UMLKSK CUI: C0009676
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanTBP6908TATA box binding protein
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanSOAT16646sterol O-acyltransferase 1
INFERRED, Score=800, UMLKSK CUI: C0009676
HumanSLC22A56584solute carrier family 22 (organic cation/carnitine transporter), member 5
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanSLC2A16513solute carrier family 2 (facilitated glucose transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanFLNA2316filamin A, alpha
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanCACNA1A773calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
img OMIM, Score=1000, UMLKSK CUI: C0009676
HumanATP1A2477ATPase, Na+/K+ transporting, alpha 2 polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0009676
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0009676Confusion0self