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Details
Link-It Detail - Disease - CREST Syndrome
Debug Stats
  • ### Total Build Time: 35 ms 21.321 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 300 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=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 2.244 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=20 ms Completed: 20 ms rowSize= 10.490 KB
  • CONCEPT_RELATIONSHIPS gt=4 ms Completed: 4 ms rowSize= 6.564 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
CREST Syndrome C0206138
Definition (1)
A variant of systemic sclerosis characterized by calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (5)
img Esophageal Motility Disorders C0014858
img Raynaud Disease C0034734
img Calcinosis C0006663
img Scleroderma, Limited C0748540
img Telangiectasis C0039446
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Gastrointestinal Diseases C00171786img Esophageal Motility Disorders C0014858
img Stomatognathic Diseases C0038368img Pharyngeal Diseases C00313455img Esophageal Motility Disorders C0014858
img Otorhinolaryngologic Diseases C0029896img Pharyngeal Diseases C00313455img Esophageal Motility Disorders C0014858
img Cardiovascular Diseases C0007222img Vascular Diseases C00423735img Raynaud Disease C0034734
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255175img Calcinosis C0006663
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372745img Scleroderma, Limited C0748540
img Skin and Connective Tissue Diseases C0175166img Connective Tissue Diseases C00097825img Scleroderma, Limited C0748540
img Cardiovascular Diseases C0007222img Vascular Diseases C00423734img Telangiectasis C0039446
Relationships (14)

Relation Types:
diso_​to_​chem : 2
diso_​to_​diso : 12


Relationships:
none : 10
clinically_​similar : 1
permuted_​term_​of : 1
related_​to : 1
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO34img Complication Aspects C1171258
DISO_to_DISO28img Complication Aspects C1171258
DISO_to_DISO6img Calcinosis C0006663
DISO_to_CHEM4img Abs - Autoantibodies C0004358
DISO_to_DISO4img Biliary cirrhosis C0023892
DISO_to_DISO4img Hypertension, Pulmonary C0020542
DISO_to_CHEM3img Antibodies, Antinuclear C0003243
DISO_to_DISO3img Calcinosis C0006663
DISO_to_DISO3img Dermatologic disorders C0037274
DISO_to_DISO3img Scleroderma, Systemic C0036421
DISO_to_DISOpermuted_term_ofimg CREST Syndrome C0206138
DISO_to_DISOclinically_similarimg PROGRESSIVE SYSTEMIC SCLEROSIS INVOLVING ESOPHAGUS C0519054
DISO_to_DISOrelated_toimg SCLERODERMA, FAMILIAL PROGRESSIVE C1866983
DISO_to_DISOused_forimg Scleroderma, Systemic C0036421
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0206138CREST Syndrome0self