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Details
Link-It Detail - Disease - Esophageal Achalasia
Debug Stats
  • ### Total Build Time: 45 ms 22.778 KB
  • CONCEPT_NAME gt=16 ms Completed: 16 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 349 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=3 ms Completed: 3 ms rowSize= 565 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.102 KB
  • CONCEPT_RELATIONSHIPS gt=17 ms Completed: 17 ms rowSize= 12.997 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 3.084 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Esophageal Achalasia C0014848
Definition (1)
failure of normal relaxation of the lower esophageal sphincter associated with uncoordinated contractions of the thoracic esophagus, resulting in functional obstruction and difficulty swallowing.
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 (44)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 5
diso_​to_​diso : 27
diso_​to_​phen : 2


Relationships:
none : 29
classifies : 2
clinically_​similar : 1
isa : 2
location_​of : 2
mapped_​to : 7
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO134img Complication Aspects C1171258
DISO_to_DISO88img Complication Aspects C1171258
DISO_to_ANAT71img Esophagus C0014876
DISO_to_ANAT50img Esophagus C0014876
DISO_to_PHEN38img genetic aspects C0017399
DISO_to_PHEN37img genetic aspects C0017399
DISO_to_ANAT34img Esophageal Sphincter, Lower C0227192
DISO_to_DISO32img Deglutition Disorders C0011168
DISO_to_DISO28img Esophageal Neoplasms C0014859
DISO_to_DISO27img Lacrimal Apparatus Diseases C0022904
DISO_to_DISO23img Chagas Disease C0041234
DISO_to_DISO23img Gastroesophageal Reflux C0017168
DISO_to_ANAT22img Cardia C0007144
DISO_to_CHEM22img Botulinum Toxins C0006055
DISO_to_DISO22img Adrenal Insufficiency C0001623
DISO_to_DISO22img Deglutition Disorders C0011168
DISO_to_DISO21img Adrenal Insufficiency C0001623
DISO_to_ANAT20img Esophagogastric Junction C0014871
DISO_to_DISO20img Gastroesophageal Reflux C0017168
DISO_to_ANAT19img Cardia C0007144
DISO_to_ANAT18img Esophageal Sphincter, Lower C0227192
DISO_to_DISO18img Esophageal Neoplasms C0014859
DISO_to_ANAT17img Muscle, Smooth C1267092
DISO_to_DISO16img COMPL POSTOP C0032787
DISO_to_CHEM14img ANTIDYSKINESIA AGENTS C0242951
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img GENERIF, Score=1000, Pubmed Id: 17961776, UMLKSK CUI: C0014848
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
img OMIM, Score=1000, UMLKSK CUI: C0014848
img GENERIF, Score=861, Pubmed Id: 15843079, UMLKSK CUI: C0014848
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0014848Esophageal Achalasia0self