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Details
Link-It Detail - Disease - Alzheimer Disease
Debug Stats
  • ### Total Build Time: 245 ms 57.947 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 381 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 381 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 973 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 4.070 KB
  • CONCEPT_RELATIONSHIPS gt=179 ms Completed: 179 ms rowSize= 16.098 KB
  • CONCEPT_GENES gt=53 ms Completed: 53 ms rowSize= 34.715 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 (2)
Alzheimer Disease C0002395
Alzheimer's Disease
Definition (1)
neurodegenerative disorder of the CNS resulting in progressive loss of memory and intellectual functions; begins in the middle or later years; characterized by brain lesions such as neurofibrillary tangles and neuritic plaques.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Tauopathies C0949664
img Dementia C0497327
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neurodegenerative Diseases C05248514img Tauopathies C0949664
img Mental Disorders C0004936img Delirium, Dementia, Amnestic, Cognitive Disorders C00292274img Dementia C0497327
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Dementia C0497327
Relationships (484)

Relation Types:
diso_​to_​anat : 35
diso_​to_​chem : 227
diso_​to_​diso : 115
diso_​to_​gene : 46
diso_​to_​phen : 3
diso_​to_​phys : 58


Relationships:
none : 304
alias_​of : 1
associated_​with : 6
classifies : 2
clinically_​similar : 6
gene_​associated_​with_​disease : 43
gene_​product_​malfunction_​associated_​with_​disease : 12
is_​associated_​anatomic_​site_​of : 2
isa : 3
manifestation_​of : 6
mapped_​to : 8
may_​prevent : 13
may_​treat : 70
permuted_​term_​of : 1
related_​to : 7
Page Size
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  Page 1 of 20
Prior Page
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN2918img genetic aspects C0017399
DISO_to_PHEN2063img genetic aspects C0017399
DISO_to_CHEM2007img Amyloid beta-Peptides C0078939
DISO_to_ANAT1850img Brain C0006104
DISO_to_DISO1495img Cognition Disorders C0009241
DISO_to_DISO1340img Complication Aspects C1171258
DISO_to_CHEM1292img Amyloid beta-Peptides C0078939
DISO_to_ANAT1242img Brain C0006104
DISO_to_DISO853img Cognition Disorders C0009241
DISO_to_DISO771img Complication Aspects C1171258
DISO_to_CHEM586img Cholinesterase Inhibitors C0008425
DISO_to_CHEM586img Fragments, Peptide C0030935
DISO_to_PHYS583img Aging C0001811
DISO_to_ANAT573img In Blood C0005768
DISO_to_CHEM544img tau Proteins C0085401
DISO_to_CHEM521img Amyloid beta-Protein Precursor C0085151
DISO_to_CHEM484img Cholinesterase Inhibitors C0008425
DISO_to_ANAT476img Neurons C0027882
DISO_to_DISO475img Dementia C0497327
DISO_to_ANAT447img Hippocampus C0019564
DISO_to_CHEM442img Amyloid beta-Protein Precursor C0085151
DISO_to_ANAT406img Neurons C0027882
DISO_to_PHYS390img GENET PREDISPOSITION C0314657
DISO_to_CHEM388img Apolipoprotein E C0003595
DISO_to_PHYS382img Aging C0001811
Genes (352)

Species:
human : 352
Page Size
Current 25
  Page 1 of 15
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanAD10780912Alzheimer disease-10
img OMIM, Score=1000, UMLKSK CUI: C0002395
HumanLOC646506646506lysosomal-associated membrane protein 1 pseudogene
img GENERIF, Score=734, Pubmed Id: 16972884, UMLKSK CUI: C0002395
HumanLOC643387643387TAR DNA binding protein pseudogene
img GENERIF, Score=1000, Pubmed Id: 17963732, UMLKSK CUI: C0002395
img GENERIF, Score=1000, Pubmed Id: 17469117, UMLKSK CUI: C0002395
HumanAD9450086Alzheimer disease 9
img OMIM, Score=1000, UMLKSK CUI: C0002395
HumanMIR146A406938microRNA 146a
img GENERIF, Score=734, Pubmed Id: 18801740, UMLKSK CUI: C0002395
HumanARMS2387715age-related maculopathy susceptibility 2
img GENERIF, Score=1000, Pubmed Id: 18688167, UMLKSK CUI: C0002395
HumanAGRN375790agrin
img GENERIF, Score=1000, Pubmed Id: 12270958, UMLKSK CUI: C0002395
HumanAD8353128Alzheimer disease 8
img OMIM, Score=1000, UMLKSK CUI: C0002395
HumanLRRTM3347731leucine rich repeat transmembrane neuronal 3
img GENERIF, Score=1000, Pubmed Id: 17098871, UMLKSK CUI: C0002395
HumanSREK1IP1285672SREK1-interacting protein 1
img GENERIF, Score=734, Pubmed Id: 15456940, UMLKSK CUI: C0002395
HumanLAMA1284217laminin, alpha 1
img GENERIF, Score=694, Pubmed Id: 12111806, UMLKSK CUI: C0002395
HumanPCSK9255738proprotein convertase subtilisin/kexin type 9
img GENERIF, Score=1000, Pubmed Id: 16314752, UMLKSK CUI: C0002395
HumanCALHM1255022calcium homeostasis modulator 1
img GENERIF, Score=1000, Pubmed Id: 18585350, UMLKSK CUI: C0002395
img GENERIF, Score=734, Pubmed Id: 19070563, UMLKSK CUI: C0002395
img GENERIF, Score=1000, Pubmed Id: 19038093, UMLKSK CUI: C0002395
HumanSTH246744saitohin
img GENERIF, Score=1000, Pubmed Id: 12826738, UMLKSK CUI: C0002395
img GENERIF, Score=1000, Pubmed Id: 12932819, UMLKSK CUI: C0002395
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
img GENERIF, Score=673, Pubmed Id: 18434550, UMLKSK CUI: C0002395
HumanLRRC15131578leucine rich repeat containing 15
img GENERIF, Score=734, Pubmed Id: 16098915, UMLKSK CUI: C0002395
HumanLRRK2120892leucine-rich repeat kinase 2
img GENERIF, Score=673, Pubmed Id: 17846883, UMLKSK CUI: C0002395
img GENERIF, Score=1000, Pubmed Id: 16102903, UMLKSK CUI: C0002395
HumanCOL25A184570collagen, type XXV, alpha 1
img GENERIF, Score=1000, Pubmed Id: 16300410, UMLKSK CUI: C0002395
HumanRNF14681847ring finger protein 146
img GENERIF, Score=1000, Pubmed Id: 15813938, UMLKSK CUI: C0002395
HumanBHLHB980823basic helix-loop-helix domain containing, class B, 9
img GENERIF, Score=734, Pubmed Id: 15034937, UMLKSK CUI: C0002395
HumanCOL18A180781collagen, type XVIII, alpha 1
img GENERIF, Score=1000, Pubmed Id: 12486154, UMLKSK CUI: C0002395
img GENERIF, Score=1000, Pubmed Id: 12408231, UMLKSK CUI: C0002395
HumanPTGES280142prostaglandin E synthase 2
img GENERIF, Score=1000, Pubmed Id: 18631945, UMLKSK CUI: C0002395
HumanRTN4R65078reticulon 4 receptor
img GENERIF, Score=1000, Pubmed Id: 17188332, UMLKSK CUI: C0002395
img GENERIF, Score=694, Pubmed Id: 17182778, UMLKSK CUI: C0002395
HumanAD664851Alzheimer disease 6
img OMIM, Score=1000, UMLKSK CUI: C0002395
HumanABCG464137ATP-binding cassette, sub-family G (WHITE), member 4
img GENERIF, Score=734, Pubmed Id: 18508037, UMLKSK CUI: C0002395
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002395Alzheimer Disease0self