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Details
Link-It Detail - Disease - Brain Damage, Chronic
Debug Stats
  • ### Total Build Time: 28 ms 28.480 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 513 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=3 ms Completed: 3 ms rowSize= 550 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.403 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=11 ms Completed: 11 ms rowSize= 13.556 KB
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 9.270 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Brain Damage, Chronic C0006109
Definition (1)
A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Brain Diseases C0006111
Children (3)
img Brain Injury, Chronic C0751813
img Cerebral Palsy C0007789
img Persistent Vegetative State C0242670
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076824img Brain Diseases C0006111
Relationships (79)

Relation Types:
diso_​to_​anat : 17
diso_​to_​chem : 3
diso_​to_​diso : 41
diso_​to_​phen : 2
diso_​to_​phys : 16


Relationships:
none : 69
entry_​version_​of : 1
is_​associated_​anatomic_​site_​of : 2
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 3
mapped_​to : 3
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO60img Complication Aspects C1171258
DISO_to_DISO57img Cognition Disorders C0009241
DISO_to_DISO50img Complication Aspects C1171258
DISO_to_ANAT49img Brain C0006104
DISO_to_DISO45img Cognition Disorders C0009241
DISO_to_DISO40img chemically induced C0007994
DISO_to_DISO38img INFANT PREMATURE DIS C0021295
DISO_to_DISO34img Developmental Disabilities C0008073
DISO_to_DISO33img Brain Injuries C0270611
DISO_to_DISO29img Brain Injuries C0270611
DISO_to_DISO29img COMPL POSTOP C0032787
DISO_to_DISO29img chemically induced C0007994
DISO_to_PHYS29img Cerebral Dominance C0013010
DISO_to_DISO27img INFANT PREMATURE DIS C0021295
DISO_to_ANAT26img Frontal Lobe C0016733
DISO_to_DISO26img Perceptual Disorders C0030975
DISO_to_DISO25img Cerebrovascular accident C0038454
DISO_to_PHYS23img Functional Laterality C1720777
DISO_to_ANAT22img Hippocampus C0019564
DISO_to_ANAT21img Hippocampus C0019564
DISO_to_CHEM21img Agents, Neuroprotective C0242912
DISO_to_DISO21img Brain Ischemia C0007786
DISO_to_ANAT20img Cerebral Cortex C0007776
DISO_to_PHYS20img Performance, Psychomotor C0033923
DISO_to_DISO18img COMPL POSTOP C0032787
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanTREX111277three prime repair exonuclease 1
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanPLP15354proteolipid protein 1
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanMBL24153mannose-binding lectin (protein C) 2, soluble
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanLTA4049lymphotoxin alpha
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanIL183606interleukin 18 (interferon-gamma-inducing factor)
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanIGFBP33486insulin-like growth factor binding protein 3
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanGSR2936glutathione reductase
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanGPX42879glutathione peroxidase 4
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanF72155coagulation factor VII (serum prothrombin conversion accelerator)
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanF52153coagulation factor V (proaccelerin, labile factor)
INFERRED, Score=800, UMLKSK CUI: C0006109
HumanAPOE348apolipoprotein E
INFERRED, Score=800, UMLKSK CUI: C0006109
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0006109Brain Damage, Chronic0self