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Details
Link-It Detail - Disease - Autonomic Nervous System Diseases
Debug Stats
  • ### Total Build Time: 19 ms 38.223 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 428 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 677 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
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  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 17.301 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Autonomic Nervous System Diseases C1145628
Autonomic nervous system disorders
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of the parasympathetic or sympathetic divisions of the autonomic nervous system; autonomic dysfunction may be associated with hypothalamic diseases, brain stem disorders, spinal cord diseases, and peripheral nervous system diseases; manifestations include impairments of vegetative functions including the maintenance of blood pressure, heart rate, pupil function, sweating, reproductive and urinary physiology, and digestion.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Nervous System Diseases C0027765
Children (6)
img Adie Syndrome C0001519
img Horner Syndrome C0019937
img Autonomic Dysreflexia C0238015
img Complex Regional Pain Syndromes C0458219
img Primary Dysautonomias C0013363
img Sweating, Gustatory C0038994
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C00277652img Nervous System Diseases C0027765
Relationships (159)

Relation Types:
diso_​to_​anat : 18
diso_​to_​chem : 6
diso_​to_​diso : 121
diso_​to_​phen : 2
diso_​to_​phys : 12


Relationships:
none : 108
classified_​as : 3
classifies : 1
entry_​version_​of : 1
isa : 29
mapped_​to : 13
related_​to : 4
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO213img Complication Aspects C1171258
DISO_to_DISO212img Complication Aspects C1171258
DISO_to_DISO79img Parkinson Disease C0030567
DISO_to_DISO73img Diabetic Neuropathies C0011882
DISO_to_DISO71img Diabetic Neuropathies C0011882
DISO_to_ANAT68img Autonomic nervous system C0004388
DISO_to_ANAT58img Autonomic Nervous System C0004388
DISO_to_PHYS55img Heart Rate C0018810
DISO_to_DISO50img Cardiovascular Diseases C0007222
DISO_to_PHYS49img Heart Rate C0018810
DISO_to_ANAT39img Heart C0018787
DISO_to_ANAT39img Sympathetic Nervous System C0039044
DISO_to_DISO39img Diabetes Mellitus, Insulin-Dependent C0011854
DISO_to_DISO37img Hypotension, Orthostatic C0020651
DISO_to_DISO37img Parkinson Disease C0030567
DISO_to_PHEN36img genetic aspects C0017399
DISO_to_DISO32img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_ANAT31img Sympathetic Nervous System C0039044
DISO_to_DISO31img Arrhythmias, Cardiac C0003811
DISO_to_PHEN31img genetic aspects C0017399
DISO_to_DISO30img Cardiovascular Diseases C0007222
DISO_to_DISO30img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_DISO30img Hypertension C0020538
DISO_to_ANAT29img In Blood C0005768
DISO_to_DISO29img Diabetes Mellitus, Insulin-Dependent C0011854
Genes (70)

Species:
human : 70
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKIF6221458kinesin family member 6
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanRETN56729resistin
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanGP651206glycoprotein VI (platelet)
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanKIF1B23095kinesin family member 1B
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanHRH311255histamine receptor H3
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanPROCR10544protein C receptor, endothelial
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanPHOX2B8929paired-like homeobox 2b
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanCTNNAL18727catenin (cadherin-associated protein), alpha-like 1
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanVCAM17412vascular cell adhesion molecule 1
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanTNNI17135troponin I type 1 (skeletal, slow)
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanTNFRSF1A7132tumor necrosis factor receptor superfamily, member 1A
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanTLR47099toll-like receptor 4
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanTIMP17076TIMP metallopeptidase inhibitor 1
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanTHBD7056thrombomodulin
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanHNF1A6927HNF1 homeobox A
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanSELE6401selectin E
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanSAA26289serum amyloid A2
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanS100B6285S100 calcium binding protein B
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanS100A126283S100 calcium binding protein A12
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanREL5966v-rel avian reticuloendotheliosis viral oncogene homolog
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanMAPK35595mitogen-activated protein kinase 3
INFERRED, Score=800, UMLKSK CUI: C1145628
HumanMAPK15594mitogen-activated protein kinase 1
INFERRED, Score=800, UMLKSK CUI: C1145628
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1145628Autonomic Nervous System Diseases0self