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Details
Link-It Detail - Disease - SCA10
Debug Stats
  • ### Total Build Time: 22 ms 16.123 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 308 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=1 ms Completed: 1 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=17 ms Completed: 17 ms rowSize= 12.381 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 2.231 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.140 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
SCA10 C1963674
Relationships (30)

Relation Types:
diso_​to_​diso : 29
diso_​to_​phys : 1


Relationships:
expanded_​form_​of : 1
manifestation_​of : 29
Page Size
Current 25
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Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg ATAXIC GAIT C0751837
DISO_to_DISOmanifestation_ofimg Abnormal coordination C0520966
DISO_to_DISOmanifestation_ofimg Age at onset 14 to 44 years C1863792
DISO_to_DISOmanifestation_ofimg Appendicular Ataxia C0750937
DISO_to_DISOmanifestation_ofimg Caused by a pentanucleotide repeat expansion (ATTCT)n in the ataxin 10 gene (ATXN10, 603516.0001). C2676890
DISO_to_DISOmanifestation_ofimg Cerebellar Dysmetria C0234162
DISO_to_DISOmanifestation_ofimg Cerebellar ataxia, progressive C0393525
DISO_to_DISOmanifestation_ofimg Cerebellar atrophy C0740279
DISO_to_DISOmanifestation_ofimg DYSDIADOCHOKINESIA C0234979
DISO_to_DISOmanifestation_ofimg Deglutition Disorders C0011168
DISO_to_DISOmanifestation_ofimg Dementia C0497327
DISO_to_DISOmanifestation_ofimg Depressed mood C0344315
DISO_to_DISOmanifestation_ofimg Dysarthria C0013362
DISO_to_DISOmanifestation_ofimg Extrapyramidal sign C0234133
DISO_to_DISOmanifestation_ofimg Hyperreflexia C0151889
DISO_to_DISOmanifestation_ofimg Impaired cognition C0338656
DISO_to_DISOmanifestation_ofimg Nerve conduction abnormalities C1866772
DISO_to_DISOmanifestation_ofimg Normal alleles have 10 to 29 repeats and pathologic alleles have 400 to 4,500 repeats C1970351
DISO_to_DISOmanifestation_ofimg Nystagmus C0028738
DISO_to_DISOmanifestation_ofimg Ocular movement abnormalities C1858502
DISO_to_DISOmanifestation_ofimg Patients of Brazilian origin have a pure cerebellar atrophy C2676891
DISO_to_DISOmanifestation_ofimg Patients of Mexican or Amerindian origin have a complicated phenotype with additional neurologic features C2676892
DISO_to_DISOmanifestation_ofimg Pyramidal sign C0234132
DISO_to_DISOmanifestation_ofimg Reduced penetrance C1842571
DISO_to_DISOexpanded_form_ofimg SCA10 C1963674
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanATXN1025814ataxin 10
img GENERIF, Score=923, Pubmed Id: 16385455, UMLKSK CUI: C1963674
img GENERIF, Score=923, Pubmed Id: 18386626, UMLKSK CUI: C1963674
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1963674SCA100self