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Details
Link-It Detail - Disease - Purpura, Thrombocytopenic
Debug Stats
  • ### Total Build Time: 50 ms 35.613 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 280 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=6 ms Completed: 6 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 1.396 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.005 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 6.237 KB
  • CONCEPT_RELATIONSHIPS gt=17 ms Completed: 17 ms rowSize= 13.303 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 11.636 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Purpura, Thrombocytopenic C0857305
Thrombocytopenic purpura
Definition (1)
Any form of purpura in which the PLATELET COUNT is decreased. Many forms are thought to be caused by immunological mechanisms.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Immune System Diseases C0021053
img Purpura C0034150
img Thrombotic Microangiopathies C2717961
Children (2)
img Purpura, Thrombocytopenic, Idiopathic C0043117
img Purpura, Thrombotic Thrombocytopenic C0034155
Ancestral Roots
RootRoot Plus OneDepthParent
img Immune System Diseases C00210532img Immune System Diseases C0021053
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Purpura C0034150
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306605img Purpura C0034150
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Purpura C0034150
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189396img Thrombotic Microangiopathies C2717961
Relationships (50)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 23
diso_​to_​diso : 20


Relationships:
none : 22
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 10
mapped_​to : 2
may_​treat : 12
use : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO20img Complication Aspects C1171258
DISO_to_DISO18img Complication Aspects C1171258
DISO_to_ANAT17img In Blood C0005768
DISO_to_ANAT16img In Blood C0005768
DISO_to_DISO12img chemically induced C0007994
DISO_to_CHEM8img Immunoglobulins, Intravenous C0085297
DISO_to_CHEM7img Immunoglobulins, Intravenous C0085297
DISO_to_ANAT6img Blood Platelets C0005821
DISO_to_CHEM6img Antibodies, Monoclonal C0003250
DISO_to_CHEM6img Antigens, Human Platelet C0085355
DISO_to_DISO6img Anemia, Hemolytic, Autoimmune C0002880
DISO_to_CHEM5img Alloantibodies C0022144
DISO_to_ANAT4img Megakaryocytes C0025166
DISO_to_CHEM4img Abs - Autoantibodies C0004358
DISO_to_CHEM4img Cyclosporine C0010592
DISO_to_CHEM4img Interferon-alpha C0002199
DISO_to_CHEM4img Isoantibodies C0022144
DISO_to_CHEM4img Measles-Mumps-Rubella Vaccine C0065828
DISO_to_CHEM4img Rho(D) Immune Globulin C0073188
DISO_to_DISO4img AUTOIMMUNE DIS C0004364
DISO_to_DISO4img Brucellosis C0006309
DISO_to_DISO4img Helicobacter Infections C0079487
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanTBX2130009T-box 21
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
img GENERIF, Score=875, Pubmed Id: 12223999, UMLKSK CUI: C0857305
HumanWASF18936WAS protein family, member 1
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanWAS7454Wiskott-Aldrich syndrome
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanVWF7450von Willebrand factor
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanNFATC24773nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanCD464179CD46 molecule, complement regulatory protein
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanIL23558interleukin 2
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanCFH3075complement factor H
INFERRED, Score=800, UMLKSK CUI: C0857305
HumanFCGR3A2214Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
img GAD, Score=1000, Pubmed Id: 12492589, UMLKSK CUI: C0857305
HumanFCGR2B2213Fc fragment of IgG, low affinity IIb, receptor (CD32)
img GAD, Score=1000, Pubmed Id: 15566359, UMLKSK CUI: C0857305
HumanFCGR2A2212Fc fragment of IgG, low affinity IIa, receptor (CD32)
img GAD, Score=1000, Pubmed Id: 12492589, UMLKSK CUI: C0857305
HumanCPB21361carboxypeptidase B2 (plasma)
INFERRED, Score=800, UMLKSK CUI: C0857305
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0857305Purpura, Thrombocytopenic0self