Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Disease - von Willebrand Diseases
Debug Stats
  • ### Total Build Time: 47 ms 26.713 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 528 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 1.858 KB
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.431 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 6.729 KB
  • CONCEPT_RELATIONSHIPS gt=25 ms Completed: 25 ms rowSize= 14.380 KB
  • CONCEPT_GENES gt=1 ms Completed: 1 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
von Willebrand Diseases C0042974
von Willebrand Disease
Definition (1)
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (4)
img Hemorrhagic Disorders C0019087
img Coagulation Protein Disorders C0600503
img Blood Platelet Disorders C0005818
img Blood Coagulation Disorders, Inherited C0852077
Children (3)
img von Willebrand Disease, Type 3 C1264041
img von Willebrand Disease, Type 1 C1264039
img von Willebrand Disease, Type 2 C1264040
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Hemorrhagic Disorders C0019087
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Coagulation Protein Disorders C0600503
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Blood Platelet Disorders C0005818
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Blood Coagulation Disorders, Inherited C0852077
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501234img Blood Coagulation Disorders, Inherited C0852077
Relationships (77)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 29
diso_​to_​diso : 39
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 23
classifies : 2
clinically_​similar : 6
is_​associated_​anatomic_​site_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
isa : 5
mapped_​to : 17
may_​treat : 20
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM213img von Willebrand Factor C0042971
DISO_to_PHEN169img genetic aspects C0017399
DISO_to_ANAT148img In Blood C0005768
DISO_to_CHEM142img von Willebrand Factor C0042971
DISO_to_PHEN131img genetic aspects C0017399
DISO_to_DISO120img Complication Aspects C1171258
DISO_to_DISO115img Complication Aspects C1171258
DISO_to_ANAT87img In Blood C0005768
DISO_to_CHEM59img Factor VIII C0015506
DISO_to_DISO53img Hemorrhage C0019080
DISO_to_CHEM38img Factor VIII C0015506
DISO_to_DISO38img Hemophilia A C0019069
DISO_to_CHEM35img Deamino Arginine Vasopressin C0011701
DISO_to_CHEM33img Hemostatic Agents C0019120
DISO_to_DISO31img Hemorrhage C0019080
DISO_to_CHEM27img Deamino Arginine Vasopressin C0011701
DISO_to_PHYS27img Mutation C0026882
DISO_to_CHEM24img A69 COAGULANTS C0009117
DISO_to_PHYS23img Missense Mutation C0599155
DISO_to_DISO21img Menorrhagia C0025323
DISO_to_CHEM19img Hemostatic Agents C0019120
DISO_to_DISO19img Hemophilia A C0019069
DISO_to_DISO19img Menorrhagia C0025323
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_associated_anatomic_site_ofimg Hematopoietic and Lymphatic System C1512394
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0042974von Willebrand Diseases0self