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Details
Link-It Detail - Disease - Brain Diseases
Debug Stats
  • ### Total Build Time: 1,338 ms 50.158 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 429 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=1 ms Completed: 1 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= 567 bytes
  • CONCEPT_CHILDREN gt=46 ms Completed: 46 ms rowSize= 12.911 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.532 KB
  • CONCEPT_RELATIONSHIPS gt=478 ms Completed: 478 ms rowSize= 14.382 KB
  • CONCEPT_GENES gt=804 ms Completed: 804 ms rowSize= 18.683 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Brain Diseases C0006111
Definition (1)
Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Central Nervous System Diseases C0007682
Children (30)
img Basal Ganglia Diseases C0004782
img Leukoencephalopathies C0270612
img Brain Edema C1527311
img Encephalitis C0014038
img Brain Damage, Chronic C0006109
img Thalamic Diseases C0039726
img Brain Neoplasms C0006118
img Epilepsy C0014544
img Hydrocephalus C0020255
img Amblyopia C0002418
img Cerebellar Diseases C0007760
img Neuroaxonal Dystrophies C0338473
img Intracranial Hypotension C0524812
img Auditory Diseases, Central C0004303
img Headache Disorders C0393735
img Cerebrovascular Disorders C0007820
img Intracranial Hypertension C0151740
img Brain Diseases, Metabolic C0006112
img Hypothalamic Diseases C0020655
img Kluver-Bucy Syndrome C0270707
img Encephalomalacia C0014068
img Subdural Effusion C0038538
img Brain Injuries C0270611
img Dementia C0497327
img Diffuse Cerebral Sclerosis of Schilder C0007795
img Hypoxia, Brain C1527348
img Brain Abscess C0006105
img Akinetic Mutism C0001889
img Amnesia, Transient Global C0338591
img Brain Death C0006110
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076823img Central Nervous System Diseases C0007682
Relationships (419)

Relation Types:
diso_​to_​anat : 51
diso_​to_​chem : 23
diso_​to_​diso : 326
diso_​to_​phen : 2
diso_​to_​phys : 17


Relationships:
none : 232
associated_​with : 2
entry_​version_​of : 1
is_​associated_​anatomic_​site_​of : 2
isa : 155
location_​of : 1
mapped_​to : 16
related_​to : 10
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO546img Complication Aspects C1171258
DISO_to_ANAT542img Brain C0006104
DISO_to_DISO458img Complication Aspects C1171258
DISO_to_ANAT444img Brain C0006104
DISO_to_PHEN245img genetic aspects C0017399
DISO_to_DISO224img chemically induced C0007994
DISO_to_PHEN196img genetic aspects C0017399
DISO_to_DISO186img chemically induced C0007994
DISO_to_ANAT118img Cerebral Cortex C0007776
DISO_to_DISO117img Cyst C0010709
DISO_to_ANAT96img Cerebral Cortex C0007776
DISO_to_DISO82img Calcinosis C0006663
DISO_to_DISO79img Cyst C0010709
DISO_to_DISO75img Brain Neoplasms C0006118
DISO_to_DISO74img Mental Disorders C0004936
DISO_to_DISO72img Calcinosis C0006663
DISO_to_DISO70img Cognition Disorders C0009241
DISO_to_DISO70img Hashimoto Disease C0677607
DISO_to_DISO63img Epilepsy C0014544
DISO_to_ANAT62img In Blood C0005768
DISO_to_DISO62img Epilepsy C0014544
DISO_to_ANAT59img Neurons C0027882
DISO_to_DISO57img Mental Disorders C0004936
DISO_to_DISO56img Choristoma C0008519
DISO_to_ANAT52img Brain Stem C0006121
Genes (2079)

Species:
human : 2079
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanFASA100192455fertility associated sperm antigen
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanOCTN3100049579organic cation transporter 3
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanAD10780912Alzheimer disease-10
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanLOC729225729225
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanD2HGDH728294D-2-hydroxyglutarate dehydrogenase
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanPARK12677662Parkinson disease 12 (susceptibility)
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanLOC646506646506lysosomal-associated membrane protein 1 pseudogene
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanLOC645503645503SUMO-activating enzyme subunit 2-like
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanLOC643387643387TAR DNA binding protein pseudogene
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanC1orf190541468
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanAD9450086Alzheimer disease 9
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanMIR133B442890microRNA 133b
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanCDNF441549cerebral dopamine neurotrophic factor
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanZYG11A440590zyg-11 family member A, cell cycle regulator
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanLOC439999439999
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanEIG3432400Epilepsy, idiopathic generalized, susceptibility to 3
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanMIR212406994microRNA 212
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanMIR21406991microRNA 21
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanMIR16-1406950
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanMIR146A406938microRNA 146a
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0006111
HumanLOC401495401495
INFERRED, Score=800, UMLKSK CUI: C0006111
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0006111Brain Diseases0self