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Details
Link-It Detail - Disease - Biliary Atresia
Debug Stats
  • ### Total Build Time: 60 ms 34.463 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= 260 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= 247 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 1,002 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 4.141 KB
  • CONCEPT_RELATIONSHIPS gt=42 ms Completed: 42 ms rowSize= 13.973 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 13.371 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)
Biliary Atresia C0005411
Definition (1)
A congenital disorder characterized by blockage or absence of the intrahepatic or extrahepatic bile ducts.
Semantic Types (2)
Disease or Syndrome (T047)
Congenital Abnormality (T019)
Parents (2)
img Bile Duct Diseases C0005395
img Digestive System Abnormalities C0266015
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Biliary Tract Diseases C00054244img Bile Duct Diseases C0005395
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Digestive System Abnormalities C0266015
img Digestive System Diseases C0012242img Digestive System Abnormalities C02660153img Digestive System Abnormalities C0266015
Relationships (83)

Relation Types:
diso_​to_​anat : 18
diso_​to_​chem : 1
diso_​to_​diso : 61
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 42
associated_​with : 1
classifies : 2
inheritance_​type_​of : 1
is_​associated_​anatomic_​site_​of : 3
isa : 2
location_​of : 2
manifestation_​of : 17
mapped_​to : 13
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO86img Complication Aspects C1171258
DISO_to_DISO80img Complication Aspects C1171258
DISO_to_ANAT50img Liver C0023884
DISO_to_PHEN37img genetic aspects C0017399
DISO_to_ANAT33img In Blood C0005768
DISO_to_PHEN31img genetic aspects C0017399
DISO_to_DISO25img Liver Cirrhosis C0023890
DISO_to_ANAT24img In Blood C0005768
DISO_to_ANAT21img Liver C0023884
DISO_to_DISO17img BILIARY STASIS C0008370
DISO_to_DISO17img COMPL POSTOP C0032787
DISO_to_DISO16img BILIARY STASIS C0008370
DISO_to_DISO15img Liver Cirrhosis C0023890
DISO_to_ANAT14img Bile Ducts, Extrahepatic C0206187
DISO_to_DISO14img Abnormalities, Multiple C0000772
DISO_to_ANAT13img Bile Ducts, Extrahepatic C0206187
DISO_to_ANAT13img Portal Vein C0032718
DISO_to_DISO13img COMPL POSTOP C0032787
DISO_to_ANAT12img Bile Ducts C0005400
DISO_to_ANAT11img Bile Ducts C0005400
DISO_to_ANAT11img Bile Ducts, Intrahepatic C0005401
DISO_to_DISO11img Cholangitis C0008311
DISO_to_DISO11img Choledochal Cyst C0008340
DISO_to_DISO11img DISEASES DUE TO ROTAVIRUS C0035869
DISO_to_DISO10img Abnormalities, Multiple C0000772
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanCFC155997cripto, FRL-1, cryptic family 1
img GENERIF, Score=673, Pubmed Id: 18162845, UMLKSK CUI: C0005411
HumanTIMP17076TIMP metallopeptidase inhibitor 1
img GENERIF, Score=1000, Pubmed Id: 17136882, UMLKSK CUI: C0005411
HumanSPP16696secreted phosphoprotein 1
img GENERIF, Score=1000, Pubmed Id: 15845635, UMLKSK CUI: C0005411
HumanSELE6401selectin E
img GENERIF, Score=1000, Pubmed Id: 18704886, UMLKSK CUI: C0005411
HumanMX14599myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse)
img GENERIF, Score=1000, Pubmed Id: 17075576, UMLKSK CUI: C0005411
HumanMMP74316matrix metallopeptidase 7 (matrilysin, uterine)
img GENERIF, Score=1000, Pubmed Id: 15696117, UMLKSK CUI: C0005411
HumanMIF4282macrophage migration inhibitory factor (glycosylation-inhibiting factor)
img GAD, Score=1000, Pubmed Id: 16385258, UMLKSK CUI: C0005411
HumanICAM13383intercellular adhesion molecule 1
img GENERIF, Score=1000, Pubmed Id: 16097065, UMLKSK CUI: C0005411
img GENERIF, Score=1000, Pubmed Id: 18401716, UMLKSK CUI: C0005411
HumanCTGF1490connective tissue growth factor
img GENERIF, Score=1000, Pubmed Id: 15459777, UMLKSK CUI: C0005411
img GENERIF, Score=1000, Pubmed Id: 17375628, UMLKSK CUI: C0005411
img GENERIF, Score=734, Pubmed Id: 16291159, UMLKSK CUI: C0005411
HumanCD14929CD14 molecule
img GENERIF, Score=1000, Pubmed Id: 16061600, UMLKSK CUI: C0005411
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0005411Biliary Atresia0self