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Details
Link-It Detail - Disease - SPINOCEREBELLAR ATAXIA 17
Debug Stats
  • ### Total Build Time: 58 ms 17.271 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 348 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=53 ms Completed: 53 ms rowSize= 12.020 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 3.682 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
SPINOCEREBELLAR ATAXIA 17 C1846707
Relationships (44)

Relation Types:
diso_​to_​diso : 44


Relationships:
alias_​of : 1
manifestation_​of : 43
Page Size
Current 25
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Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg A69 APRAXIAS C0003635
DISO_to_DISOmanifestation_ofimg Aggression C0001807
DISO_to_DISOmanifestation_ofimg Appendicular Ataxia C0750937
DISO_to_DISOmanifestation_ofimg Axial rigidity C1846708
DISO_to_DISOmanifestation_ofimg Bradykinesia C0233565
DISO_to_DISOmanifestation_ofimg Broad-based gait C1836917
DISO_to_DISOmanifestation_ofimg Caused by a trinucleotide repeat expansion (CAG)n in the TATA box-binding protein gene (TBP, 600075.0001) C2675937
DISO_to_DISOmanifestation_ofimg Cerebellar Dysmetria C0234162
DISO_to_DISOmanifestation_ofimg Cerebellar atrophy C0740279
DISO_to_DISOmanifestation_ofimg Chorea C0008489
DISO_to_DISOmanifestation_ofimg Deglutition Disorders C0011168
DISO_to_DISOmanifestation_ofimg Dementia C0497327
DISO_to_DISOmanifestation_ofimg Dementia, frontal lobe C1846712
DISO_to_DISOmanifestation_ofimg Depressed mood C0344315
DISO_to_DISOmanifestation_ofimg Diffuse cerebral atrophy C0598275
DISO_to_DISOmanifestation_ofimg Disorientation C0233407
DISO_to_DISOmanifestation_ofimg Dysarthria C0013362
DISO_to_DISOmanifestation_ofimg Dystonia C0013421
DISO_to_DISOmanifestation_ofimg Frontal release signs C1836153
DISO_to_DISOmanifestation_ofimg Gait Ataxia C0751837
DISO_to_DISOmanifestation_ofimg Gaze-evoked nystagmus (33%) C1969723
DISO_to_DISOmanifestation_ofimg Gliosis in the striatum, medial thalamic nuclei, and inferior olives C1846710
DISO_to_DISOmanifestation_ofimg Hallucinations C0018524
DISO_to_DISOmanifestation_ofimg Impaired pursuit initiation and maintenance C1969722
DISO_to_DISOmanifestation_ofimg Incontinence (in late stages) C1846713
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanTBP6908TATA box binding protein
img GENERIF, Score=923, Pubmed Id: 17149738, UMLKSK CUI: C1846707
img GENERIF, Score=700, Pubmed Id: 17846415, UMLKSK CUI: C1846707
img GENERIF, Score=1000, Pubmed Id: 14978680, UMLKSK CUI: C1846707
img GENERIF, Score=722, Pubmed Id: 14763955, UMLKSK CUI: C1846707
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1846707SPINOCEREBELLAR ATAXIA 170self