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Details
Link-It Detail - Disease - SPINOCEREBELLAR ATAXIA 29
Debug Stats
  • ### Total Build Time: 30 ms 8.379 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=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=20 ms Completed: 20 ms rowSize= 4.967 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 1.843 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
SPINOCEREBELLAR ATAXIA 29 C1861732
Relationships (11)

Relation Types:
diso_​to_​diso : 11


Relationships:
expanded_​form_​of : 1
manifestation_​of : 10
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Atrophy of the cerebellar vermis on MRI C1861734
DISO_to_DISOmanifestation_ofimg Broad-based gait C1836917
DISO_to_DISOmanifestation_ofimg Cerebellar ataxia, nonprogressive C1845029
DISO_to_DISOmanifestation_ofimg Cognitive impairment, mild (reported in 1 large family) C1861733
DISO_to_DISOmanifestation_ofimg DYSDIADOCHOKINESIA C0234979
DISO_to_DISOmanifestation_ofimg Delay in motor development C1864913
DISO_to_DISOmanifestation_ofimg Dysarthria C0013362
DISO_to_DISOmanifestation_ofimg Highly variable phenotype C1865012
DISO_to_DISOmanifestation_ofimg Nystagmus C0028738
DISO_to_DISOmanifestation_ofimg Onset at birth C1836142
DISO_to_DISOexpanded_form_ofimg SPINOCEREBELLAR ATAXIA 29 C1861732
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanCEP29080184centrosomal protein 290kDa
img OMIM, Score=1000, UMLKSK CUI: C1861732
img OMIM, Score=1000, UMLKSK CUI: C1861732
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1861732SPINOCEREBELLAR ATAXIA 290self