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Details
Link-It Detail - Disease - Celiac Disease
Debug Stats
  • ### Total Build Time: 328 ms 21.217 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 414 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=16 ms Completed: 16 ms rowSize= 559 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=12 ms Completed: 12 ms rowSize= 2.809 KB
  • CONCEPT_RELATIONSHIPS gt=284 ms Completed: 284 ms rowSize= 15.729 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Celiac Disease C0007570
Definition (1)
A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Malabsorption Syndromes C0024523
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Gastrointestinal Diseases C00171785img Malabsorption Syndromes C0024523
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Malabsorption Syndromes C0024523
Relationships (202)

Relation Types:
diso_​to_​anat : 22
diso_​to_​chem : 35
diso_​to_​diso : 129
diso_​to_​gene : 4
diso_​to_​phen : 3
diso_​to_​phys : 9


Relationships:
none : 115
associated_​with : 3
classifies : 1
expanded_​form_​of : 1
gene_​associated_​with_​disease : 2
gene_​product_​malfunction_​associated_​with_​disease : 1
inheritance_​type_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 4
location_​of : 1
manifestation_​of : 56
mapped_​to : 8
may_​treat : 1
related_​to : 7
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO804img Complication Aspects C1171258
DISO_to_DISO715img Complication Aspects C1171258
DISO_to_PHEN335img genetic aspects C0017399
DISO_to_PHEN258img genetic aspects C0017399
DISO_to_ANAT205img In Blood C0005768
DISO_to_DISO194img Diet, Gluten-Free C0344351
DISO_to_CHEM188img Transglutaminases C0033679
DISO_to_CHEM181img Transglutaminases C0033679
DISO_to_CHEM180img Gluten Proteins C0017842
DISO_to_CHEM180img Glutens C0017842
DISO_to_CHEM178img Gluten Proteins C0017842
DISO_to_CHEM166img Abs - Autoantibodies C0004358
DISO_to_CHEM166img Autoantibodies C0004358
DISO_to_CHEM164img Abs - Autoantibodies C0004358
DISO_to_ANAT162img Intestinal Mucosa C0021839
DISO_to_ANAT160img In Blood C0005768
DISO_to_CHEM140img Gliadin C0017622
DISO_to_CHEM114img Immunoglobulin A C0020835
DISO_to_ANAT113img Duodenum C0013303
DISO_to_DISO107img Diabetes Mellitus, Insulin-Dependent C0011854
DISO_to_ANAT100img Intestinal Mucosa C0021839
DISO_to_CHEM86img Gliadin C0017622
DISO_to_ANAT85img Intestine, Small C0021852
DISO_to_DISO84img Diabetes Mellitus, Insulin-Dependent C0011854
DISO_to_CHEM83img Immunoglobulin A C0020835
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0007570Celiac Disease0self