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Details
Link-It Detail - Disease - Purpura, Thrombotic Thrombocytopenic
Debug Stats
  • ### Total Build Time: 96 ms 32.290 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 370 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 243 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=3 ms Completed: 3 ms rowSize= 992 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=17 ms Completed: 17 ms rowSize= 7.968 KB
  • CONCEPT_RELATIONSHIPS gt=46 ms Completed: 45 ms rowSize= 13.518 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 7.849 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Purpura, Thrombotic Thrombocytopenic C0034155
Definition (1)
a kind of blood disorder that causes blood clots to form in blood vessels around the body
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Thrombophilia C0398623
img Purpura, Thrombocytopenic C0857305
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Thrombophilia C0398623
img Immune System Diseases C0021053img Purpura, Thrombocytopenic C08573053img Purpura, Thrombocytopenic C0857305
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Purpura, Thrombocytopenic C0857305
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189396img Purpura, Thrombocytopenic C0857305
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306606img Purpura, Thrombocytopenic C0857305
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189397img Purpura, Thrombocytopenic C0857305
Relationships (42)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 19
diso_​to_​diso : 15
diso_​to_​phen : 2


Relationships:
none : 32
clinically_​similar : 2
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 2
isa : 2
mapped_​to : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM123img A Disintegrin and Metalloprotease Proteins C1566416
DISO_to_CHEM123img ADAM Proteins C1566416
DISO_to_DISO122img Complication Aspects C1171258
DISO_to_DISO114img Complication Aspects C1171258
DISO_to_DISO108img Hemolytic-Uremic Syndrome C0019061
DISO_to_ANAT106img In Blood C0005768
DISO_to_CHEM105img Metalloendopeptidases C1442934
DISO_to_ANAT97img In Blood C0005768
DISO_to_DISO73img Hemolytic-Uremic Syndrome C0019061
DISO_to_PHEN59img genetic aspects C0017399
DISO_to_CHEM52img A Disintegrin and Metalloprotease Proteins C1566416
DISO_to_PHEN51img genetic aspects C0017399
DISO_to_DISO41img chemically induced C0007994
DISO_to_CHEM39img Antibodies, Monoclonal C0003250
DISO_to_CHEM38img von Willebrand Factor C0042971
DISO_to_CHEM37img Antibodies, Monoclonal C0003250
DISO_to_DISO28img Lupus Erythematosus, Systemic C0024141
DISO_to_DISO27img COMPL HEMATOL PREGN C0032964
DISO_to_CHEM26img von Willebrand Factor C0042971
DISO_to_DISO25img Lupus Erythematosus, Systemic C0024141
DISO_to_CHEM24img Immunologic Factors C0021054
DISO_to_CHEM22img Abs - Autoantibodies C0004358
DISO_to_CHEM19img Antibodies, Monoclonal, Murine-Derived C2916903
DISO_to_CHEM18img Immunosuppressive Agents C0021081
DISO_to_DISO17img COMPL HEMATOL PREGN C0032964
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
img GENERIF, Score=1000, Pubmed Id: 18668574, UMLKSK CUI: C0034155
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
img OMIM, Score=1000, UMLKSK CUI: C0034155
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
Click here to display 29 evidence detail records.
HumanVWF7450von Willebrand factor
img GENERIF, Score=1000, Pubmed Id: 14727254, UMLKSK CUI: C0034155
HumanCD464179CD46 molecule, complement regulatory protein
img OMIM, Score=1000, UMLKSK CUI: C0034155
img OMIM, Score=1000, UMLKSK CUI: C0034155
HumanCFH3075complement factor H
img OMIM, Score=1000, UMLKSK CUI: C0034155
img OMIM, Score=1000, UMLKSK CUI: C0034155
HumanCPB21361carboxypeptidase B2 (plasma)
img GENERIF, Score=983, Pubmed Id: 17327284, UMLKSK CUI: C0034155
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0034155Purpura, Thrombotic Thrombocytopenic0self