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Details
Link-It Detail - Disease - Blood Platelet Disorders
Debug Stats
  • ### Total Build Time: 132 ms 38.611 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 346 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 218 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 3.119 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=53 ms Completed: 53 ms rowSize= 13.414 KB
  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 18.100 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Blood Platelet Disorders C0005818
Definition (1)
Disorders caused by abnormalities in platelet count or function.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Hematologic Diseases C0018939
Children (7)
img Thrombocytosis C0836924
img Platelet Storage Pool Deficiency C0032197
img Thrombasthenia C0040015
img Bernard-Soulier Syndrome C0005129
img von Willebrand Diseases C0042974
img Thrombocytopenia C0040034
img Gray Platelet Syndrome C0272302
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189393img Hematologic Diseases C0018939
Relationships (33)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 4
diso_​to_​diso : 21
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 18
associated_​with : 1
isa : 7
location_​of : 1
mapped_​to : 1
permuted_​term_​of : 1
related_​to : 3
use : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN56img genetic aspects C0017399
DISO_to_ANAT53img In Blood C0005768
DISO_to_ANAT43img Blood Platelets C0005821
DISO_to_DISO42img Complication Aspects C1171258
DISO_to_PHEN34img genetic aspects C0017399
DISO_to_ANAT29img In Blood C0005768
DISO_to_ANAT28img Blood Platelets C0005821
DISO_to_PHYS23img Platelet Aggregation C0032176
DISO_to_DISO21img Complication Aspects C1171258
DISO_to_DISO18img Hemorrhage C0019080
DISO_to_DISO15img chemically induced C0007994
DISO_to_DISO13img Thrombocytopenia C0040034
DISO_to_DISO11img Blood Coagulation Disorders C0005779
DISO_to_CHEM9img Deamino Arginine Vasopressin C0011701
DISO_to_CHEM8img Platelet Aggregation Inhibitors C0032177
DISO_to_CHEM8img von Willebrand Factor C0042971
DISO_to_DISO8img Blood Coagulation Disorders C0005779
DISO_to_DISO8img von Willebrand Disease C0042974
DISO_to_ANATlocation_ofimg Blood Platelets C0005821
DISO_to_CHEMrelated_toimg Anticoagulants C0003280
DISO_to_DISOisaimg Acquired PF-3 disease C1261263
DISO_to_DISOisaimg Acquired platelet disorder C0398636
DISO_to_DISOrelated_toimg Bleeding tendency C1458140
DISO_to_DISOpermuted_term_ofimg Blood Platelet Disorders C0005818
DISO_to_DISOrelated_toimg Blood and Blood Disorders C1456636
Genes (155)

Species:
human : 155
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanPPBPL1728045
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanERVK7449619
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanSTOX1219736storkhead box 1
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanMASTL84930microtubule associated serine/threonine kinase-like
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanCFHR581494complement factor H-related 5
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanVPS33A65082vacuolar protein sorting 33 homolog A (S. cerevisiae)
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanSLEB364695systemic lupus erythematosus susceptibility 3
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanDCLRE1C64421DNA cross-link repair 1C
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanCD17757126CD177 molecule
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanC10orf256652chromosome 10 open reading frame 2
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanNOP1055505NOP10 ribonucleoprotein
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanBANK155024B-cell scaffold protein with ankyrin repeats 1
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanCYCS54205cytochrome c, somatic
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanA4GALT53947alpha 1,4-galactosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanGP651206glycoprotein VI (platelet)
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanSLC45A251151solute carrier family 45, member 2
INFERRED, Score=800, UMLKSK CUI: C0005818
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
INFERRED, Score=800, UMLKSK CUI: C0005818
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0005818Blood Platelet Disorders0self