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Details
Link-It Detail - Disease - Basal Ganglia Diseases
Debug Stats
  • ### Total Build Time: 56 ms 41.305 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 342 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 528 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=0 Completed: 0 ms rowSize= 550 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 5.329 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 13.180 KB
  • CONCEPT_GENES gt=54 ms Completed: 54 ms rowSize= 18.526 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Basal Ganglia Diseases C0004782
Definition (1)
Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Brain Diseases C0006111
Children (12)
img Dystonia Musculorum Deformans C0013423
img Supranuclear Palsy, Progressive C0038868
img Tourette Syndrome C0040517
img Huntington Disease C0020179
img Basal Ganglia Cerebrovascular Disease C0751739
img Hepatolenticular Degeneration C0019202
img Parkinsonian Disorders C0242422
img Chorea Gravidarum C0264746
img Pantothenate Kinase-Associated Neurodegeneration C0018523
img Multiple System Atrophy C0393571
img Neuroleptic Malignant Syndrome C0027849
img Meige Syndrome C0025183
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076824img Brain Diseases C0006111
Relationships (86)

Relation Types:
diso_​to_​anat : 9
diso_​to_​chem : 8
diso_​to_​diso : 66
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 55
isa : 21
mapped_​to : 8
permuted_​term_​of : 1
used_​for : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO125img chemically induced C0007994
DISO_to_CHEM88img ANTIPSYCHOTICS C0040615
DISO_to_DISO88img chemically induced C0007994
DISO_to_DISO67img Calcinosis C0006663
DISO_to_PHEN63img genetic aspects C0017399
DISO_to_CHEM58img ANTIPSYCHOTICS C0040615
DISO_to_DISO56img Complication Aspects C1171258
DISO_to_PHEN56img genetic aspects C0017399
DISO_to_DISO49img Complication Aspects C1171258
DISO_to_DISO47img Calcinosis C0006663
DISO_to_DISO41img Schizophrenia C0036341
DISO_to_ANAT33img Basal Ganglia C0004781
DISO_to_DISO27img Schizophrenia C0036341
DISO_to_DISO25img Neurodegenerative Diseases C0524851
DISO_to_ANAT22img Basal Ganglia C0004781
DISO_to_DISO19img Dementia C0497327
DISO_to_DISO17img Psychotic Disorders C0033975
DISO_to_ANAT16img Brain C0006104
DISO_to_ANAT16img Corpus Striatum C0010097
DISO_to_DISO16img Movement Disorders C0026650
DISO_to_DISO16img Neurodegenerative Diseases C0524851
DISO_to_DISO15img Dyskinesia, Drug-Induced C0013386
DISO_to_ANAT14img Brain C0006104
DISO_to_ANAT14img Cerebral Cortex C0007776
DISO_to_DISO14img Psychotic Disorders C0033975
Genes (595)

Species:
human : 595
Page Size
Current 25
  Page 1 of 24
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFASA100192455fertility associated sperm antigen
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanAD10780912Alzheimer disease-10
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanLOC729225729225
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanPARK12677662Parkinson disease 12 (susceptibility)
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanC1orf190541468
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanAD9450086Alzheimer disease 9
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanMIR133B442890microRNA 133b
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanCDNF441549cerebral dopamine neurotrophic factor
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanZYG11A440590zyg-11 family member A, cell cycle regulator
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanHSP90AB2P391634heat shock protein 90kDa alpha (cytosolic), class B member 2, pseudogene
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanSKINTL391037Skint-like, pseudogene
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanLDLRAD1388633low density lipoprotein receptor class A domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanLOC388630388630
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanC1orf175374977
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanAD8353128Alzheimer disease 8
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanFAM159A348378family with sequence similarity 159, member A
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanKIAA1267284058
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanCYP4X1260293cytochrome P450, family 4, subfamily X, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanNEGR1257194neuronal growth regulator 1
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanPCSK9255738proprotein convertase subtilisin/kexin type 9
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanANKK1255239ankyrin repeat and kinase domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanSTH246744saitohin
INFERRED, Score=800, UMLKSK CUI: C0004782
HumanMTIF3219402mitochondrial translational initiation factor 3
INFERRED, Score=800, UMLKSK CUI: C0004782
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0004782Basal Ganglia Diseases0self