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Details
Link-It Detail - Disease - Disease
Debug Stats
  • ### Total Build Time: 4,119 ms 37.695 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 350 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=2 ms Completed: 2 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 546 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.530 KB
  • CONCEPT_RELATIONSHIPS gt=545 ms Completed: 545 ms rowSize= 14.019 KB
  • CONCEPT_GENES gt=3,555 ms Completed: 3.555 Seconds rowSize= 19.071 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Disease C0012634
Definition (1)
A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Pathologic Processes C0030660
Children (1)
img Syndrome C0039082
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306603img Pathologic Processes C0030660
Relationships (484)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 13
diso_​to_​diso : 425
diso_​to_​gene : 6
diso_​to_​phen : 5
diso_​to_​phys : 33


Relationships:
none : 82
associated_​with : 306
entry_​version_​of : 1
isa : 94
use : 1
Page Size
Current 25
  Page 1 of 20
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN524img genetic aspects C0017399
DISO_to_PHYS64img GENET PREDISPOSITION C0314657
DISO_to_GENE46img Polymorphism, Single Nucleotide C0752046
DISO_to_PHYS43img Aging C0001811
DISO_to_PHYS40img Signal Transduction C0037083
DISO_to_CHEM39img Proteins C0033684
DISO_to_PHYS36img Epigenesis, Genetic C1257873
DISO_to_CHEM33img MicroRNAs C1101610
DISO_to_PHYS33img Mutation C0026882
DISO_to_CHEM29img Proteins C0033684
DISO_to_PHEN28img Genetic Variation C0042333
DISO_to_GENE26img Genome, Human C0017429
DISO_to_PHYS25img Aging C0001811
DISO_to_PHYS25img Gene Regulatory Networks C1720950
DISO_to_PHYS24img Gene Expression Regulation C0017263
DISO_to_DISO19img Diagnosis C0011900
DISO_to_PHEN18img EVOLUTION MOL C0282688
DISO_to_DISO17img Environmental Exposure C0014412
DISO_to_PHYS16img Biological Evolution C0015219
DISO_to_PHYS15img Signal Transduction C0037083
DISO_to_DISO13img Animal Disease Models C0012644
DISO_to_DISO12img DELAYED EFF PRENATAL EXPOSURE C0033054
DISO_to_DISO12img Diagnosis C0011900
DISO_to_DISO12img Life Stress C0038443
DISO_to_DISO12img Oxidative Stress C0242606
Genes (7768)

Species:
human : 7768
Page Size
Current 25
  Page 1 of 311
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanFASA100192455fertility associated sperm antigen
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanBMND8100188854bone mineral density quantiative trait locus 8
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanBMND7100188853bone mineral density quantiative trait locus 7
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanNIDDM4100188782Diabetes mellitus, noninsulin-dependent
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanCD24100133941CD24 molecule
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanLOC100133284100133284striatin, calmodulin binding protein pseudogene
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanSPANXB2100133171SPANX family, member B2
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanKIR2DS2100132285killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanNCRNA00271100131814
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanPSORS1C3100130889psoriasis susceptibility 1 candidate 3 (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanCTAGE4100128553CTAGE family, member 4
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanZGLP1100125288zinc finger, GATA-like protein 1
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanOCTN3100049579organic cation transporter 3
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanTPP2827833tripeptidyl peptidase II
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanDFNB72791116
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanAD10780912Alzheimer disease-10
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanHAR1A768096highly accelerated region 1A (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanLOC732093732093
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanDIRC3729582disrupted in renal carcinoma 3
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanLOC729249729249
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanLOC729225729225
INFERRED, Score=800, UMLKSK CUI: C0012634
HumanLOC729177729177
INFERRED, Score=800, UMLKSK CUI: C0012634
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0012634Disease0self