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Details
Link-It Detail - Disease - Confusion Adverse Event
Debug Stats
  • ### Total Build Time: 14 ms 15.475 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=6 ms Completed: 6 ms rowSize= 2.495 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 11.416 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Confusion Adverse Event C1963086
Relationships (5)

Relation Types:
diso_​to_​diso : 5


Relationships:
isa : 5
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOisaimg CTCAE Grade 1 Confusion C1561307
DISO_to_DISOisaimg CTCAE Grade 2 Confusion C1561308
DISO_to_DISOisaimg CTCAE Grade 3 Confusion C1561309
DISO_to_DISOisaimg CTCAE Grade 4 Confusion C1561310
DISO_to_DISOisaimg CTCAE Grade 5 Confusion C1561311
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanNAGS162417N-acetylglutamate synthase
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanAMN81693amnion associated transmembrane protein
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanSLC25A1510166solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
img OMIM, Score=833, UMLKSK CUI: C1963086
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanTKT7086transketolase
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanSLC22A56584solute carrier family 22 (organic cation/carnitine transporter), member 5
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanSLC2A16513solute carrier family 2 (facilitated glucose transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanCACNA1A773calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
img OMIM, Score=1000, UMLKSK CUI: C1963086
HumanATP1A2477ATPase, Na+/K+ transporting, alpha 2 polypeptide
img OMIM, Score=1000, UMLKSK CUI: C1963086
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1963086Confusion Adverse Event0self