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 - Behcet Syndrome
Debug Stats
  • ### Total Build Time: 75 ms 63.475 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 522 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=4 ms Completed: 4 ms rowSize= 1.812 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=16 ms Completed: 16 ms rowSize= 5.305 KB
  • CONCEPT_RELATIONSHIPS gt=36 ms Completed: 36 ms rowSize= 14.427 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 39.733 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Behcet Syndrome C0004943
Definition (1)
Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (4)
img Mouth Diseases C0026636
img Vasculitis C0042384
img Uveitis, Anterior C0042165
img Skin Diseases, Vascular C0162819
Ancestral Roots
RootRoot Plus OneDepthParent
img Stomatognathic Diseases C0038368img Mouth Diseases C00266363img Mouth Diseases C0026636
img Cardiovascular Diseases C0007222img Vascular Diseases C00423734img Vasculitis C0042384
img Eye Diseases C0015397img Uveal Diseases C00421616img Uveitis, Anterior C0042165
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372744img Skin Diseases, Vascular C0162819
Relationships (126)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 24
diso_​to_​diso : 87
diso_​to_​gene : 2
diso_​to_​phen : 2
diso_​to_​phys : 5


Relationships:
none : 97
associated_​with : 12
classifies : 1
isa : 4
mapped_​to : 5
may_​treat : 5
mth_​has_​plain_​text_​form : 1
related_​to : 1
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO559img Complication Aspects C1171258
DISO_to_DISO540img Complication Aspects C1171258
DISO_to_PHEN172img genetic aspects C0017399
DISO_to_ANAT140img In Blood C0005768
DISO_to_PHEN134img genetic aspects C0017399
DISO_to_ANAT112img In Blood C0005768
DISO_to_CHEM93img Antibodies, Monoclonal C0003250
DISO_to_CHEM56img Immunosuppressive Agents C0021081
DISO_to_CHEM53img Anti-Inflammatory Agents C0003209
DISO_to_DISO52img Uveitis C0042164
DISO_to_DISO46img Aneurysm C0002940
DISO_to_DISO44img Aneurysm C0002940
DISO_to_GENE44img Polymorphism, Single Nucleotide C0752046
DISO_to_PHYS39img Genetic Polymorphism C0032529
DISO_to_CHEM38img Tumor Necrosis Factor-alpha C1456820
DISO_to_CHEM37img Immunosuppressive Agents C0021081
DISO_to_CHEM36img Antibodies, Monoclonal C0003250
DISO_to_ANAT34img Pulmonary Artery C0034052
DISO_to_DISO34img Thrombosis C0040053
DISO_to_DISO30img Venous Thrombosis C0042487
DISO_to_ANAT29img Pulmonary Artery C0034052
DISO_to_CHEM29img Tumor Necrosis Factor-alpha C1456820
DISO_to_DISO29img Thrombosis C0040053
DISO_to_PHYS28img Genetic Polymorphism C0032529
DISO_to_DISO27img Intestinal Diseases C0021831
Genes (67)

Species:
human : 67
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
img GENERIF, Score=1000, Pubmed Id: 12918694, UMLKSK CUI: C0004943
img GENERIF, Score=901, Pubmed Id: 12373294, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 12068141, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 15272769, UMLKSK CUI: C0004943
img GENERIF, Score=734, Pubmed Id: 16784494, UMLKSK CUI: C0004943
img GENERIF, Score=694, Pubmed Id: 12918695, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 16767211, UMLKSK CUI: C0004943
HumanSUMO4387082small ubiquitin-like modifier 4
img GENERIF, Score=1000, Pubmed Id: 18657476, UMLKSK CUI: C0004943
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img GENERIF, Score=1000, Pubmed Id: 15515785, UMLKSK CUI: C0004943
HumanTLR954106toll-like receptor 9
img GENERIF, Score=1000, Pubmed Id: 17854429, UMLKSK CUI: C0004943
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img GENERIF, Score=1000, Pubmed Id: 17868256, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 17660222, UMLKSK CUI: C0004943
HumanTNFSF13B10673tumor necrosis factor (ligand) superfamily, member 13b
img GENERIF, Score=901, Pubmed Id: 19026118, UMLKSK CUI: C0004943
HumanCXCL1310563chemokine (C-X-C motif) ligand 13
img GENERIF, Score=734, Pubmed Id: 17949547, UMLKSK CUI: C0004943
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
img GENERIF, Score=1000, Pubmed Id: 17949565, UMLKSK CUI: C0004943
HumanPROZ8858protein Z, vitamin K-dependent plasma glycoprotein
img GENERIF, Score=1000, Pubmed Id: 14507116, UMLKSK CUI: C0004943
HumanVWF7450von Willebrand factor
img GENERIF, Score=660, Pubmed Id: 15849757, UMLKSK CUI: C0004943
HumanVEGFA7422vascular endothelial growth factor A
img GENERIF, Score=901, Pubmed Id: 15338501, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 18204875, UMLKSK CUI: C0004943
HumanTXK7294TXK tyrosine kinase
img GENERIF, Score=1000, Pubmed Id: 16809408, UMLKSK CUI: C0004943
HumanTNFRSF1B7133tumor necrosis factor receptor superfamily, member 1B
img GENERIF, Score=756, Pubmed Id: 12918703, UMLKSK CUI: C0004943
img GENERIF, Score=827, Pubmed Id: 18415772, UMLKSK CUI: C0004943
HumanTNF7124tumor necrosis factor
img GENERIF, Score=1000, Pubmed Id: 19026135, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 17657677, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 16891799, UMLKSK CUI: C0004943
img GENERIF, Score=734, Pubmed Id: 16897113, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 19026125, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 14727453, UMLKSK CUI: C0004943
HumanTLR47099toll-like receptor 4
img GENERIF, Score=1000, Pubmed Id: 18408113, UMLKSK CUI: C0004943
img GENERIF, Score=1000, Pubmed Id: 18234118, UMLKSK CUI: C0004943
HumanTLR27097toll-like receptor 2
img GENERIF, Score=734, Pubmed Id: 17934735, UMLKSK CUI: C0004943
HumanTHBD7056thrombomodulin
img GENERIF, Score=1000, Pubmed Id: 12918732, UMLKSK CUI: C0004943
HumanTRG@6965
img GENERIF, Score=1000, Pubmed Id: 12918704, UMLKSK CUI: C0004943
HumanTRD@6964
img GENERIF, Score=1000, Pubmed Id: 12918704, UMLKSK CUI: C0004943
HumanSOD26648superoxide dismutase 2, mitochondrial
img GENERIF, Score=1000, Pubmed Id: 17296902, UMLKSK CUI: C0004943
HumanSLC11A16556solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1
img GENERIF, Score=1000, Pubmed Id: 17062442, UMLKSK CUI: C0004943
HumanSELL6402selectin L
img GENERIF, Score=1000, Pubmed Id: 12918706, UMLKSK CUI: C0004943
HumanCXCL126387chemokine (C-X-C motif) ligand 12
img GENERIF, Score=734, Pubmed Id: 17949547, UMLKSK CUI: C0004943
HumanCCL216366chemokine (C-C motif) ligand 21
img GENERIF, Score=1000, Pubmed Id: 17949547, UMLKSK CUI: C0004943
HumanSAG6295S-antigen; retina and pineal gland (arrestin)
img GENERIF, Score=673, Pubmed Id: 18685727, UMLKSK CUI: C0004943
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0004943Behcet Syndrome0self