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Details
Link-It Detail - Disease - Central Nervous System Diseases
Debug Stats
  • ### Total Build Time: 619 ms 40.903 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 360 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 379 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=2 ms Completed: 2 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 559 bytes
  • CONCEPT_CHILDREN gt=16 ms Completed: 16 ms rowSize= 4.406 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.115 KB
  • CONCEPT_RELATIONSHIPS gt=262 ms Completed: 262 ms rowSize= 13.856 KB
  • CONCEPT_GENES gt=327 ms Completed: 327 ms rowSize= 18.882 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Central Nervous System Diseases C0007682
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Nervous System Diseases C0027765
Children (10)
img Pneumocephalus C0032268
img Leukoencephalopathies C0270612
img High Pressure Neurological Syndrome C0019537
img Meningitis C0025289
img Movement Disorders C0026650
img Encephalomyelitis C0014070
img Brain Diseases C0006111
img Ocular Motility Disorders C0028850
img Spinal Cord Diseases C0037928
img Central Nervous System Infections C0007684
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C00277652img Nervous System Diseases C0027765
Relationships (213)

Relation Types:
diso_​to_​anat : 28
diso_​to_​chem : 37
diso_​to_​diso : 132
diso_​to_​phen : 2
diso_​to_​phys : 14


Relationships:
none : 160
associated_​with : 5
is_​associated_​anatomic_​site_​of : 2
isa : 41
mapped_​to : 3
use : 2
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO144img Complication Aspects C1171258
DISO_to_DISO118img Complication Aspects C1171258
DISO_to_ANAT88img Central Nervous System C0927232
DISO_to_DISO86img chemically induced C0007994
DISO_to_PHEN85img genetic aspects C0017399
DISO_to_DISO80img chemically induced C0007994
DISO_to_PHEN64img genetic aspects C0017399
DISO_to_ANAT56img Brain C0006104
DISO_to_DISO53img Sarcoidosis C0036202
DISO_to_ANAT52img Central Nervous System C0927232
DISO_to_DISO45img Peripheral Nervous System Diseases C0031117
DISO_to_ANAT40img Brain C0006104
DISO_to_DISO36img Inflammation C0021368
DISO_to_DISO33img Peripheral Nervous System Diseases C0031117
DISO_to_DISO32img HIV Infections C0019693
DISO_to_CHEM29img Central Nervous System Agents C0007680
DISO_to_DISO29img Mental Disorders C0004936
DISO_to_DISO28img DEMYELINATING DIS C0011303
DISO_to_PHYS25img Nerve Regeneration C0027756
DISO_to_ANAT24img Neurons C0027882
DISO_to_DISO23img Inflammation C0021368
DISO_to_ANAT22img In Blood C0005768
DISO_to_ANAT21img Neurons C0027882
DISO_to_CHEM21img Agents, Neuroprotective C0242912
DISO_to_DISO21img Dog Diseases C0012979
Genes (2337)

Species:
human : 2337
Page Size
Current 25
  Page 1 of 94
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanFASA100192455fertility associated sperm antigen
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanOCTN3100049579organic cation transporter 3
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanAD10780912Alzheimer disease-10
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanLOC729225729225
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanD2HGDH728294D-2-hydroxyglutarate dehydrogenase
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanPARK12677662Parkinson disease 12 (susceptibility)
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanLOC647859647859occludin pseudogene
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanLOC646506646506lysosomal-associated membrane protein 1 pseudogene
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanLOC645503645503SUMO-activating enzyme subunit 2-like
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanLOC643387643387TAR DNA binding protein pseudogene
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanC1orf190541468
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanADHD4450090Attention deficit-hyperactivity disorder, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanADHD3450089Attention deficit-hyperactivity disorder, susceptibility to, 2
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanADHD2450088Attention deficit-hyperactivity disorder, susceptibility to, 2
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanADHD1450087Attention deficit-hyperactivity disorder, susceptibility to, 1
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanAD9450086Alzheimer disease 9
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanMIR133B442890microRNA 133b
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanCDNF441549cerebral dopamine neurotrophic factor
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanZYG11A440590zyg-11 family member A, cell cycle regulator
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanLOC439999439999
INFERRED, Score=800, UMLKSK CUI: C0007682
HumanEIG3432400Epilepsy, idiopathic generalized, susceptibility to 3
INFERRED, Score=800, UMLKSK CUI: C0007682
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0007682Central Nervous System Diseases0self