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 - Budd-Chiari Syndrome
Debug Stats
  • ### Total Build Time: 74 ms 24.001 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 442 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=2 ms Completed: 2 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=7 ms Completed: 7 ms rowSize= 985 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=19 ms Completed: 19 ms rowSize= 2.771 KB
  • CONCEPT_RELATIONSHIPS gt=27 ms Completed: 27 ms rowSize= 13.122 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 5.011 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Budd-Chiari Syndrome C0856761
Definition (1)
A condition in which the hepatic venous outflow is obstructed anywhere from the small HEPATIC VEINS to the junction of the INFERIOR VENA CAVA and the RIGHT ATRIUM. Usually the blockage is extrahepatic and caused by blood clots (THROMBUS) or fibrous webs. Parenchymal FIBROSIS is uncommon.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Liver Diseases C0023895
img Venous Thrombosis C0042487
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Liver Diseases C00238953img Liver Diseases C0023895
img Cardiovascular Diseases C0007222img Vascular Diseases C00423736img Venous Thrombosis C0042487
Relationships (37)

Relation Types:
diso_​to_​anat : 11
diso_​to_​chem : 3
diso_​to_​diso : 20
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 28
associated_​with : 2
classifies : 2
clinically_​similar : 1
location_​of : 2
permuted_​term_​of : 1
related_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO85img Complication Aspects C1171258
DISO_to_DISO71img Complication Aspects C1171258
DISO_to_ANAT58img Inferior vena cava structure C0042458
DISO_to_ANAT38img Inferior vena cava structure C0042458
DISO_to_ANAT32img Hepatic Veins C0019155
DISO_to_DISO30img Venous Thrombosis C0042487
DISO_to_PHEN29img genetic aspects C0017399
DISO_to_ANAT26img Portal Vein C0032718
DISO_to_PHEN26img genetic aspects C0017399
DISO_to_DISO24img Liver Neoplasms C0023903
DISO_to_DISO19img Carcinoma, Hepatocellular C2239176
DISO_to_ANAT18img Liver C0023884
DISO_to_CHEM18img Janus Kinase 2 C0169661
DISO_to_DISO17img Venous Thrombosis C0042487
DISO_to_DISO15img Liver Neoplasms C0023903
DISO_to_ANAT14img In Blood C0005768
DISO_to_CHEM14img Anticoagulants C0003280
DISO_to_DISO13img Ascites C0003962
DISO_to_DISO13img Thrombosis C0040053
DISO_to_ANAT12img In Blood C0005768
DISO_to_ANAT12img Liver C0023884
DISO_to_ANAT11img Hepatic Veins C0019155
DISO_to_CHEM11img Factor V C0015498
DISO_to_DISO11img Liver Diseases C0023895
DISO_to_PHYS11img Mutation C0026882
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanMTHFR4524methylenetetrahydrofolate reductase (NAD(P)H)
img GENERIF, Score=1000, Pubmed Id: 12221667, UMLKSK CUI: C0856761
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
img OMIM, Score=1000, UMLKSK CUI: C0856761
HumanJAK23717Janus kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0856761
img GENERIF, Score=923, Pubmed Id: 17849060, UMLKSK CUI: C0856761
HumanF52153coagulation factor V (proaccelerin, labile factor)
img GENERIF, Score=1000, Pubmed Id: 14697963, UMLKSK CUI: C0856761
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0856761Budd-Chiari Syndrome0self