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Details
Link-It Detail - Disease - Plummer-Vinson Syndrome
Debug Stats
  • ### Total Build Time: 17 ms 10.369 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 357 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=2 ms Completed: 2 ms rowSize= 565 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 4.102 KB
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 3.611 KB
  • CONCEPT_GENES gt=1 ms Completed: 1 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Plummer-Vinson Syndrome C0032249
Definition (1)
A syndrome of DYSPHAGIA with IRON-DEFICIENCY ANEMIA that is due to congenital anomalies in the ESOPHAGUS (such as cervical esophageal webs). It is known as Patterson-Kelly syndrome in the United Kingdom.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Esophageal Motility Disorders C0014858
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Gastrointestinal Diseases C00171786img Esophageal Motility Disorders C0014858
img Otorhinolaryngologic Diseases C0029896img Pharyngeal Diseases C00313455img Esophageal Motility Disorders C0014858
img Stomatognathic Diseases C0038368img Pharyngeal Diseases C00313455img Esophageal Motility Disorders C0014858
Relationships (6)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 5


Relationships:
none : 2
associated_​with : 2
location_​of : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO9img Complication Aspects C1171258
DISO_to_DISO4img Complication Aspects C1171258
DISO_to_ANATlocation_ofimg Esophagus C0014876
DISO_to_DISOassociated_withimg Abnormal deglutition C0232519
DISO_to_DISOassociated_withimg Acquired stenosis C0009814
DISO_to_DISOpermuted_term_ofimg Plummer-Vinson Syndrome C0032249
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0032249Plummer-Vinson Syndrome0self