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Details
Link-It Detail - Disease - Memory impairment
Debug Stats
  • ### Total Build Time: 18 ms 31.744 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 217 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=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 29.883 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Memory impairment C0233794
Definition (1)
A disorder characterized by a deterioration in memory function.
Genes (32)

Species:
human : 32
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDAOA267012D-amino acid oxidase activator
img GENERIF, Score=734, Pubmed Id: 17767147, UMLKSK CUI: C0233794
HumanRTN4R65078reticulon 4 receptor
img GENERIF, Score=884, Pubmed Id: 17182778, UMLKSK CUI: C0233794
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanADCK356997aarF domain containing kinase 3
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanAPTX54840aprataxin
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanCOQ227235coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanPDSS123590prenyl (decaprenyl) diphosphate synthase, subunit 1
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanNCSTN23385nicastrin
img GAD, Score=1000, Pubmed Id: 15567563, UMLKSK CUI: C0233794
HumanWWC123286WW and C2 domain containing 1
img GENERIF, Score=1000, Pubmed Id: 18378080, UMLKSK CUI: C0233794
HumanALDH5A17915aldehyde dehydrogenase 5 family, member A1
img GAD, Score=1000, Pubmed Id: 14981524, UMLKSK CUI: C0233794
HumanTKT7086transketolase
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanSPG76687spastic paraplegia 7 (pure and complicated autosomal recessive)
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanSPAST6683spastin
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanSOD16647superoxide dismutase 1, soluble
img GENERIF, Score=1000, Pubmed Id: 15288122, UMLKSK CUI: C0233794
HumanPSEN15663presenilin 1
img GAD, Score=1000, Pubmed Id: 11755019, UMLKSK CUI: C0233794
HumanPRNP5621prion protein
img GAD, Score=1000, Pubmed Id: 14593432, UMLKSK CUI: C0233794
HumanSERPINI15274serpin peptidase inhibitor, clade I (neuroserpin), member 1
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
img GAD, Score=1000, Pubmed Id: 15016421, UMLKSK CUI: C0233794
HumanHTR2A33565-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
img GAD, Score=1000, Pubmed Id: 15891581, UMLKSK CUI: C0233794
img GENERIF, Score=677, Pubmed Id: 14566344, UMLKSK CUI: C0233794
HumanGRM32913glutamate receptor, metabotropic 3
img GENERIF, Score=901, Pubmed Id: 17636131, UMLKSK CUI: C0233794
HumanECM11893extracellular matrix protein 1
img OMIM, Score=1000, UMLKSK CUI: C0233794
HumanDRD41815dopamine receptor D4
img GENERIF, Score=886, Pubmed Id: 17239353, UMLKSK CUI: C0233794
HumanDRD21813dopamine receptor D2
img GENERIF, Score=901, Pubmed Id: 17113268, UMLKSK CUI: C0233794
HumanCOMT1312catechol-O-methyltransferase
img GENERIF, Score=901, Pubmed Id: 17636131, UMLKSK CUI: C0233794
img GENERIF, Score=901, Pubmed Id: 17113268, UMLKSK CUI: C0233794
HumanCHRNA71139cholinergic receptor, nicotinic, alpha 7 (neuronal)
img GENERIF, Score=1000, Pubmed Id: 18307030, UMLKSK CUI: C0233794
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0233794Memory impairment0self