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Details
Link-It Detail - Disease - Gliosis
Debug Stats
  • ### Total Build Time: 35 ms 43.582 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 371 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 309 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= 232 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.530 KB
  • CONCEPT_RELATIONSHIPS gt=12 ms Completed: 12 ms rowSize= 12.753 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 26.688 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Gliosis C0017639
Astrocytic cell proliferation
Definition (1)
The production of a dense fibrous network of neuroglia; includes astrocytosis, which is a proliferation of astrocytes in the area of a degenerative lesion.
Semantic Types (2)
Finding (T033)
Pathologic Function (T046)
Parents (1)
img Pathologic Processes C0030660
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306603img Pathologic Processes C0030660
Relationships (80)

Relation Types:
diso_​to_​anat : 21
diso_​to_​chem : 16
diso_​to_​diso : 33
diso_​to_​phen : 2
diso_​to_​phys : 8


Relationships:
none : 78
isa : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT97img Astrocytes C0004112
DISO_to_ANAT85img Gitter cell C0206116
DISO_to_ANAT82img Gitter cell C0206116
DISO_to_ANAT74img Astrocytes C0004112
DISO_to_DISO54img Encephalitis C0014038
DISO_to_PHEN50img genetic aspects C0017399
DISO_to_DISO49img chemically induced C0007994
DISO_to_DISO45img chemically induced C0007994
DISO_to_ANAT40img Brain C0006104
DISO_to_ANAT39img Brain C0006104
DISO_to_DISO39img Brain Injuries C0270611
DISO_to_ANAT37img Neuroglia C0027836
DISO_to_PHEN35img genetic aspects C0017399
DISO_to_ANAT29img Neurons C0027882
DISO_to_DISO26img Brain Injuries C0270611
DISO_to_DISO26img Degeneration, Nerve C0027746
DISO_to_DISO24img Degeneration, Nerve C0027746
DISO_to_ANAT23img Cerebral Cortex C0007776
DISO_to_ANAT22img Hippocampus C0019564
DISO_to_ANAT19img Neurons C0027882
DISO_to_ANAT19img Retina C0035298
DISO_to_DISO19img Alzheimer Disease C0002395
DISO_to_DISO19img Spinal Cord Injuries C0037929
DISO_to_ANAT18img Neuroglia C0027836
DISO_to_DISO17img Brain Ischemia C0007786
Genes (44)

Species:
human : 44
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanC8orf38137682
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanLRRK2120892leucine-rich repeat kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanL2HGDH79944L-2-hydroxyglutarate dehydrogenase
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanSLC17A757030solute carrier family 17 (vesicular glutamate transporter), member 7
img GENERIF, Score=1000, Pubmed Id: 15961236, UMLKSK CUI: C0017639
HumanTREM254209triggering receptor expressed on myeloid cells 2
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanLRPPRC10128leucine-rich pentatricopeptide repeat containing
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanSCO29997SCO2 cytochrome c oxidase assembly protein
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanEIF2B58893eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanEIF2B28892eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanEIF2B38891eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanEIF2B48890eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanTYROBP7305TYRO protein tyrosine kinase binding protein
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanTBP6908TATA box binding protein
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanSURF16834surfeit 1
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanSDHA6389succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanCCL26347chemokine (C-C motif) ligand 2
img GENERIF, Score=827, Pubmed Id: 16733654, UMLKSK CUI: C0017639
HumanSCN1B6324sodium channel, voltage-gated, type I, beta subunit
img GENERIF, Score=660, Pubmed Id: 12677453, UMLKSK CUI: C0017639
HumanS100B6285S100 calcium binding protein B
img GENERIF, Score=827, Pubmed Id: 18451356, UMLKSK CUI: C0017639
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C0017639
img GENERIF, Score=827, Pubmed Id: 18413481, UMLKSK CUI: C0017639
HumanPOLG5428polymerase (DNA directed), gamma
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanSERPINI15274serpin peptidase inhibitor, clade I (neuroserpin), member 1
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanPDHA15160pyruvate dehydrogenase (lipoamide) alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0017639
HumanPARK25071parkinson protein 2, E3 ubiquitin protein ligase (parkin)
img OMIM, Score=1000, UMLKSK CUI: C0017639
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0017639Gliosis0self