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Details
Link-It Detail - Disease - Pyramidal sign
Debug Stats
  • ### Total Build Time: 16 ms 21.229 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 326 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=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 19.589 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Pyramidal sign C0234132
Genes (23)

Species:
human : 23
SpeciesGeneGeneIdGene NameEvidence
HumanFAM126A84668family with sequence similarity 126, member A
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanL2HGDH79944L-2-hydroxyglutarate dehydrogenase
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanCHMP2B25978charged multivesicular body protein 2B
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanATXN1025814ataxin 10
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanFBXO725793F-box protein 7
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanATP13A223400ATPase type 13A2
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanCCT522948chaperonin containing TCP1, subunit 5 (epsilon)
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanSLC25A1510166solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanMFN29927mitofusin 2
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanGPR569289G protein-coupled receptor 56
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanCTDP19150CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanGAN8139gigaxonin
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanSPG76687spastic paraplegia 7 (pure and complicated autosomal recessive)
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanSPAST6683spastin
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanATXN8OS6315ATXN8 opposite strand (non-protein coding)
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanATXN76314ataxin 7
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanATXN34287ataxin 3
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanMAPT4137microtubule-associated protein tau
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanLMNB14001lamin B1
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanKCNC33748potassium voltage-gated channel, Shaw-related subfamily, member 3
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanHSPD13329heat shock 60kDa protein 1 (chaperonin)
img OMIM, Score=1000, UMLKSK CUI: C0234132
HumanCOL4A11282collagen, type IV, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0234132
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0234132Pyramidal sign0self