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Details
Link-It Detail - Disease - Brown Tendon Sheath Syndrome
Debug Stats
  • ### Total Build Time: 13 ms 21.864 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 354 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=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 20.183 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Brown Tendon Sheath Syndrome C0155339
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanHPS489781Hermansky-Pudlak syndrome 4
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanHPS384343Hermansky-Pudlak syndrome 3
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanDTNBP184062dystrobrevin binding protein 1
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanHPS679803Hermansky-Pudlak syndrome 6
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanXYLT264132xylosyltransferase II
img OMIM, Score=666, UMLKSK CUI: C0155339
HumanXYLT164131xylosyltransferase I
img OMIM, Score=666, UMLKSK CUI: C0155339
HumanHPS511234Hermansky-Pudlak syndrome 5
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanKLK49622kallikrein-related peptidase 4
img OMIM, Score=666, UMLKSK CUI: C0155339
HumanMMP209313matrix metallopeptidase 20
img OMIM, Score=666, UMLKSK CUI: C0155339
HumanHERC28924HECT and RLD domain containing E3 ubiquitin protein ligase 2
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanOCA24948oculocutaneous albinism II
img OMIM, Score=833, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=833, UMLKSK CUI: C0155339
HumanHPS13257Hermansky-Pudlak syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0155339
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanGBA2629glucosidase, beta, acid
img OMIM, Score=666, UMLKSK CUI: C0155339
HumanDSPP1834dentin sialophosphoprotein
img OMIM, Score=666, UMLKSK CUI: C0155339
HumanATP2A2488ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
img OMIM, Score=1000, UMLKSK CUI: C0155339
HumanABCC6368ATP-binding cassette, sub-family C (CFTR/MRP), member 6
img OMIM, Score=666, UMLKSK CUI: C0155339
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0155339Brown Tendon Sheath Syndrome0self