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Details
Link-It Detail - Disease - Complex Regional Pain Syndromes
Debug Stats
  • ### Total Build Time: 38 ms 56.015 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 759 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= 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= 1,021 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 993 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.828 KB
  • CONCEPT_RELATIONSHIPS gt=11 ms Completed: 11 ms rowSize= 12.665 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 36.053 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Complex Regional Pain Syndromes C0458219
CRPS
Definition (1)
Conditions characterized by pain involving an extremity or other body region, HYPERESTHESIA, and localized autonomic dysfunction following injury to soft tissue or nerve. The pain is usually associated with ERYTHEMA; SKIN TEMPERATURE changes, abnormal sudomotor activity (i.e., changes in sweating due to altered sympathetic innervation) or edema. The degree of pain and other manifestations is out of proportion to that expected from the inciting event. Two subtypes of this condition have been described: type I; (REFLEX SYMPATHETIC DYSTROPHY) and type II; (CAUSALGIA). (From Pain 1995 Oct;63(1):127-33)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Peripheral Nervous System Diseases C0031117
img Autonomic Nervous System Diseases C1145628
Children (2)
img Causalgia C0007462
img Reflex Sympathetic Dystrophy C0034931
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neuromuscular Diseases C00278684img Peripheral Nervous System Diseases C0031117
img Nervous System Diseases C0027765img Autonomic Nervous System Diseases C11456283img Autonomic Nervous System Diseases C1145628
Relationships (53)

Relation Types:
diso_​to_​anat : 11
diso_​to_​chem : 13
diso_​to_​diso : 28
diso_​to_​phen : 1


Relationships:
none : 39
isa : 4
mapped_​to : 1
may_​treat : 6
related_​to : 3
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO43img Complication Aspects C1171258
DISO_to_CHEM19img Ketamine C0022614
DISO_to_DISO17img Complication Aspects C1171258
DISO_to_DISO17img Pain C0030193
DISO_to_CHEM15img Analgesics C0002771
DISO_to_DISO15img Pain C0030193
DISO_to_ANAT10img Spinal Cord C0037925
DISO_to_DISO10img Dystonia C0013421
DISO_to_PHEN10img genetic aspects C0017399
DISO_to_DISO9img Cerebrovascular accident C0038454
DISO_to_DISO9img Hyperalgesia C0020429
DISO_to_ANAT8img Cortex, Somatosensory C0037658
DISO_to_ANAT8img In Blood C0005768
DISO_to_ANAT8img Spinal Cord C0037925
DISO_to_ANAT7img Hand C0018563
DISO_to_ANAT7img In Blood C0005768
DISO_to_DISO7img Fibromyalgia C0016053
DISO_to_DISO7img Hyperalgesia C0020429
DISO_to_DISO7img Perceptual Disorders C0030975
DISO_to_ANAT6img Hand C0018563
DISO_to_CHEM6img Cytokines C0079189
DISO_to_DISO6img Dystonia Disorders C0393593
DISO_to_DISO6img PAIN SENSITIVITY C0162703
DISO_to_ANAT5img Brain C0006104
DISO_to_ANAT5img Cortex, Motor C0026607
Genes (53)

Species:
human : 53
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKIF6221458kinesin family member 6
img GENERIF, Score=661, Pubmed Id: 18222355, UMLKSK CUI: C0458219
HumanRETN56729resistin
img GENERIF, Score=966, Pubmed Id: 18023360, UMLKSK CUI: C0458219
HumanGP651206glycoprotein VI (platelet)
img GENERIF, Score=661, Pubmed Id: 12560230, UMLKSK CUI: C0458219
HumanPROCR10544protein C receptor, endothelial
img GENERIF, Score=827, Pubmed Id: 16153429, UMLKSK CUI: C0458219
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
img GENERIF, Score=966, Pubmed Id: 17011566, UMLKSK CUI: C0458219
img GENERIF, Score=966, Pubmed Id: 18362454, UMLKSK CUI: C0458219
img GENERIF, Score=827, Pubmed Id: 18288276, UMLKSK CUI: C0458219
img GENERIF, Score=827, Pubmed Id: 17714716, UMLKSK CUI: C0458219
img GENERIF, Score=779, Pubmed Id: 18160463, UMLKSK CUI: C0458219
HumanVCAM17412vascular cell adhesion molecule 1
img GENERIF, Score=966, Pubmed Id: 16002075, UMLKSK CUI: C0458219
img GENERIF, Score=827, Pubmed Id: 17714716, UMLKSK CUI: C0458219
HumanTNNI17135troponin I type 1 (skeletal, slow)
img GENERIF, Score=966, Pubmed Id: 16916777, UMLKSK CUI: C0458219
HumanTNFRSF1A7132tumor necrosis factor receptor superfamily, member 1A
img GENERIF, Score=1000, Pubmed Id: 16043808, UMLKSK CUI: C0458219
HumanTNF7124tumor necrosis factor
img GENERIF, Score=937, Pubmed Id: 18055234, UMLKSK CUI: C0458219
img GENERIF, Score=901, Pubmed Id: 18596918, UMLKSK CUI: C0458219
HumanTHBD7056thrombomodulin
img GENERIF, Score=827, Pubmed Id: 16153429, UMLKSK CUI: C0458219
HumanHNF1A6927HNF1 homeobox A
img GENERIF, Score=661, Pubmed Id: 18439552, UMLKSK CUI: C0458219
HumanSELE6401selectin E
img GENERIF, Score=966, Pubmed Id: 11882337, UMLKSK CUI: C0458219
img GENERIF, Score=966, Pubmed Id: 17991470, UMLKSK CUI: C0458219
HumanSAA26289serum amyloid A2
img GENERIF, Score=966, Pubmed Id: 18385816, UMLKSK CUI: C0458219
HumanS100B6285S100 calcium binding protein B
img GENERIF, Score=966, Pubmed Id: 17348038, UMLKSK CUI: C0458219
HumanREL5966v-rel avian reticuloendotheliosis viral oncogene homolog
img GENERIF, Score=661, Pubmed Id: 17335903, UMLKSK CUI: C0458219
HumanMAPK35595mitogen-activated protein kinase 3
img GENERIF, Score=661, Pubmed Id: 17615382, UMLKSK CUI: C0458219
img GENERIF, Score=661, Pubmed Id: 17652082, UMLKSK CUI: C0458219
HumanMAPK15594mitogen-activated protein kinase 1
img GENERIF, Score=661, Pubmed Id: 17615382, UMLKSK CUI: C0458219
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
img GENERIF, Score=966, Pubmed Id: 18299469, UMLKSK CUI: C0458219
HumanOLR14973oxidized low density lipoprotein (lectin-like) receptor 1
img GENERIF, Score=966, Pubmed Id: 15472120, UMLKSK CUI: C0458219
HumanNPPB4879natriuretic peptide B
img GENERIF, Score=661, Pubmed Id: 17149558, UMLKSK CUI: C0458219
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
img GENERIF, Score=966, Pubmed Id: 18675273, UMLKSK CUI: C0458219
HumanCD464179CD46 molecule, complement regulatory protein
img GENERIF, Score=694, Pubmed Id: 17412968, UMLKSK CUI: C0458219
HumanLTA4049lymphotoxin alpha
img GENERIF, Score=661, Pubmed Id: 15306179, UMLKSK CUI: C0458219
HumanLEPR3953leptin receptor
img GENERIF, Score=661, Pubmed Id: 17615382, UMLKSK CUI: C0458219
HumanLEP3952leptin
img GENERIF, Score=661, Pubmed Id: 17615382, UMLKSK CUI: C0458219
img GENERIF, Score=966, Pubmed Id: 17141244, UMLKSK CUI: C0458219
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0458219Complex Regional Pain Syndromes0self