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Details
Link-It Detail - Disease - Impaired cognition
Debug Stats
  • ### Total Build Time: 84 ms 34.098 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 229 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=18 ms Completed: 18 ms rowSize= 3.377 KB
  • CONCEPT_GENES gt=46 ms Completed: 46 ms rowSize= 28.948 KB
  • CONCEPT_XREFS gt=11 ms Completed: 11 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Impaired cognition C0338656
Definition (1)
a condition where a person has problems with the ability to think and learn
Relationships (7)

Relation Types:
diso_​to_​diso : 7


Relationships:
isa : 6
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOisaimg Age-related cognitive decline C0236848
DISO_to_DISOused_forimg Cognition Disorders C0009241
DISO_to_DISOisaimg Disturbance of cognitive learning C1291720
DISO_to_DISOisaimg Impaired cognition C0338656
DISO_to_DISOisaimg Lack of reasoning ability C1291714
DISO_to_DISOisaimg Memory impairment C0233794
DISO_to_DISOisaimg Minimal cognitive impairment C1291708
Genes (75)

Species:
human : 75
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCD24100133941CD24 molecule
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanDAOA267012D-amino acid oxidase activator
img GENERIF, Score=1000, Pubmed Id: 16554747, UMLKSK CUI: C0338656
HumanANKK1255239ankyrin repeat and kinase domain containing 1
img GENERIF, Score=983, Pubmed Id: 12151753, UMLKSK CUI: C0338656
HumanLRRK2120892leucine-rich repeat kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img GENERIF, Score=1000, Pubmed Id: 18079167, UMLKSK CUI: C0338656
HumanPANK280025pantothenate kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanPCDH1957526protocadherin 19
img GENERIF, Score=1000, Pubmed Id: 18469813, UMLKSK CUI: C0338656
HumanC10orf256652chromosome 10 open reading frame 2
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanAPTX54840aprataxin
img GENERIF, Score=901, Pubmed Id: 18202221, UMLKSK CUI: C0338656
HumanPDE11A50940phosphodiesterase 11A
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanATXN1025814ataxin 10
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanNPC210577Niemann-Pick disease, type C2
img GENERIF, Score=901, Pubmed Id: 12447927, UMLKSK CUI: C0338656
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanTSC17248tuberous sclerosis 1
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanSYP6855synaptophysin
img GENERIF, Score=1000, Pubmed Id: 16721760, UMLKSK CUI: C0338656
HumanSPAST6683spastin
img GENERIF, Score=1000, Pubmed Id: 16828199, UMLKSK CUI: C0338656
img GAD, Score=1000, Pubmed Id: 12925368, UMLKSK CUI: C0338656
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanSOAT16646sterol O-acyltransferase 1
img GENERIF, Score=1000, Pubmed Id: 17593314, UMLKSK CUI: C0338656
HumanSNCA6622synuclein, alpha (non A4 component of amyloid precursor)
img GENERIF, Score=1000, Pubmed Id: 18413475, UMLKSK CUI: C0338656
HumanSLC6A46532solute carrier family 6 (neurotransmitter transporter), member 4
img GENERIF, Score=983, Pubmed Id: 17970527, UMLKSK CUI: C0338656
img GENERIF, Score=884, Pubmed Id: 18647635, UMLKSK CUI: C0338656
HumanSELP6403selectin P (granule membrane protein 140kDa, antigen CD62)
img GENERIF, Score=1000, Pubmed Id: 17498578, UMLKSK CUI: C0338656
HumanSDHA6389succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanATXN76314ataxin 7
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanATXN16310ataxin 1
img OMIM, Score=1000, UMLKSK CUI: C0338656
HumanRPS6KA36197ribosomal protein S6 kinase, 90kDa, polypeptide 3
img GENERIF, Score=1000, Pubmed Id: 14678837, UMLKSK CUI: C0338656
HumanPTPRC5788protein tyrosine phosphatase, receptor type, C
img OMIM, Score=1000, UMLKSK CUI: C0338656
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0338656Impaired cognition0self