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Details
Link-It Detail - Disease - Autosomal Dominant Hereditary Spastic Paraplegia
Debug Stats
  • ### Total Build Time: 23 ms 16.098 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 394 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=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 14.357 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.182 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Autosomal Dominant Hereditary Spastic Paraplegia C0751602
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanSPG19140907spastic paraplegia 19 (autosomal dominant)
img GENERIF, Score=717, Pubmed Id: 12112072, UMLKSK CUI: C0751602
HumanNIPA1123606non imprinted in Prader-Willi/Angelman syndrome 1
img GENERIF, Score=1000, Pubmed Id: 14508710, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 17928003, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 15711826, UMLKSK CUI: C0751602
HumanATL151062atlastin GTPase 1
img GENERIF, Score=1000, Pubmed Id: 14607301, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 12112092, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 16339213, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 15477516, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 16401858, UMLKSK CUI: C0751602
HumanSPAST6683spastin
img OMIM, Score=1000, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 12163196, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 14732620, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 15841487, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 16788734, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 15482961, UMLKSK CUI: C0751602
img GENERIF, Score=1000, Pubmed Id: 12124993, UMLKSK CUI: C0751602
HumanKIF5A3798kinesin family member 5A
img GENERIF, Score=947, Pubmed Id: 16489470, UMLKSK CUI: C0751602
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0751602Autosomal Dominant Hereditary Spastic Paraplegia0self