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Details
Link-It Detail - Disease - Fatigue
Debug Stats
  • ### Total Build Time: 80 ms 44.563 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 321 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=0 Completed: 0 ms rowSize= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 552 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.526 KB
  • CONCEPT_RELATIONSHIPS gt=63 ms Completed: 63 ms rowSize= 14.160 KB
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 25.830 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Fatigue C0015672
Definition (1)
The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Signs and Symptoms C0037088
Children (1)
img Mental Fatigue C0015676
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370883img Signs and Symptoms C0037088
Relationships (214)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 18
diso_​to_​diso : 163
diso_​to_​phen : 2
diso_​to_​phys : 25


Relationships:
none : 119
disease_​may_​have_​finding : 70
isa : 9
mapped_​to : 1
may_​treat : 8
parent_​is_​cdrh : 1
related_​to : 1
use : 5
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO307img Neoplasms C0027651
DISO_to_DISO229img Neoplasms C0027651
DISO_to_DISO206img Complication Aspects C1171258
DISO_to_DISO154img Multiple Sclerosis C0026769
DISO_to_DISO147img Depression C0011570
DISO_to_DISO143img Pain C0030193
DISO_to_DISO136img Breast Neoplasms C1458155
DISO_to_DISO121img Sleep Disorders C0851578
DISO_to_ANAT104img In Blood C0005768
DISO_to_DISO104img Depression C0011570
DISO_to_DISO99img Life Stress C0038443
DISO_to_DISO84img Multiple Sclerosis C0026769
DISO_to_DISO81img Complication Aspects C1171258
DISO_to_DISO79img chemically induced C0007994
DISO_to_DISO78img DIS OCCUP C0028797
DISO_to_PHYS73img Sleep C0037313
DISO_to_DISO65img Breast Neoplasms C1458155
DISO_to_DISO64img Pain C0030193
DISO_to_DISO64img chemically induced C0007994
DISO_to_DISO63img Arthritis, Rheumatoid C0003873
DISO_to_DISO61img DIS OCCUP C0028797
DISO_to_CHEM58img Central Nervous System Stimulants C0002763
DISO_to_DISO56img Sleep Deprivation C0037316
DISO_to_DISO55img Life Stress C0038443
DISO_to_DISO50img Cerebrovascular accident C0038454
Genes (26)

Species:
human : 26
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPNKD25953paroxysmal nonkinesigenic dyskinesia
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanKCNE310008potassium voltage-gated channel, Isk-related family, member 3
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanWISP38838WNT1 inducible signaling pathway protein 3
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanDYSF8291dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)
img OMIM, Score=833, UMLKSK CUI: C0015672
HumanVHL7428von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanTNF7124tumor necrosis factor
img GENERIF, Score=812, Pubmed Id: 15124762, UMLKSK CUI: C0015672
HumanSLC2A16513solute carrier family 2 (facilitated glucose transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanSCN4A6329sodium channel, voltage-gated, type IV, alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanMVK4598mevalonate kinase
img OMIM, Score=833, UMLKSK CUI: C0015672
HumanKCNMA13778potassium large conductance calcium-activated channel, subfamily M, alpha member 1
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanKCNA13736potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia)
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanIL63569interleukin 6 (interferon, beta 2)
img GENERIF, Score=1000, Pubmed Id: 18082358, UMLKSK CUI: C0015672
HumanGLA2717galactosidase, alpha
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanGCH12643GTP cyclohydrolase 1
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanGABRA12554gamma-aminobutyric acid (GABA) A receptor, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanEPOR2057erythropoietin receptor
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanACE1636angiotensin I converting enzyme
img GENERIF, Score=1000, Pubmed Id: 15686789, UMLKSK CUI: C0015672
HumanCOMT1312catechol-O-methyltransferase
img GENERIF, Score=660, Pubmed Id: 18936597, UMLKSK CUI: C0015672
HumanCLCN21181chloride channel, voltage-sensitive 2
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanCHAT1103choline O-acetyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanSERPINA6866serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6
img GENERIF, Score=1000, Pubmed Id: 17547679, UMLKSK CUI: C0015672
HumanCACNB4785calcium channel, voltage-dependent, beta 4 subunit
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanCACNA1S779calcium channel, voltage-dependent, L type, alpha 1S subunit
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanCACNA1A773calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
img OMIM, Score=1000, UMLKSK CUI: C0015672
HumanATP1B3483ATPase, Na+/K+ transporting, beta 3 polypeptide
img GENERIF, Score=861, Pubmed Id: 17446412, UMLKSK CUI: C0015672
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015672Fatigue0self