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Details
Link-It Detail - Disease - Congenital myopathy (disorder)
Debug Stats
  • ### Total Build Time: 9 ms 11.011 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 358 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=6 ms Completed: 6 ms rowSize= 9.323 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Congenital myopathy (disorder) C0270960
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanTPM37170tropomyosin 3
img OMIM, Score=882, UMLKSK CUI: C0270960
HumanTPM27169tropomyosin 2 (beta)
img OMIM, Score=882, UMLKSK CUI: C0270960
HumanRYR16261ryanodine receptor 1 (skeletal)
img GENERIF, Score=1000, Pubmed Id: 12136074, UMLKSK CUI: C0270960
img GENERIF, Score=651, Pubmed Id: 12112081, UMLKSK CUI: C0270960
img GENERIF, Score=861, Pubmed Id: 15564033, UMLKSK CUI: C0270960
HumanHRAS3265Harvey rat sarcoma viral oncogene homolog
img GENERIF, Score=694, Pubmed Id: 17412879, UMLKSK CUI: C0270960
HumanCNTN11272contactin 1
img GENERIF, Score=901, Pubmed Id: 19026398, UMLKSK CUI: C0270960
HumanCFL21073cofilin 2 (muscle)
img GENERIF, Score=1000, Pubmed Id: 17160903, UMLKSK CUI: C0270960
HumanACTA158actin, alpha 1, skeletal muscle
img OMIM, Score=882, UMLKSK CUI: C0270960
img GENERIF, Score=861, Pubmed Id: 15520409, UMLKSK CUI: C0270960
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0270960Congenital myopathy (disorder)0self