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Details
Link-It Detail - Disease - Deglutition Disorders
Debug Stats
  • ### Total Build Time: 348 ms 44.763 KB
  • CONCEPT_NAME gt=18 ms Completed: 17 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 176 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=13 ms Completed: 13 ms rowSize= 992 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 567 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=32 ms Completed: 32 ms rowSize= 4.072 KB
  • CONCEPT_RELATIONSHIPS gt=229 ms Completed: 229 ms rowSize= 14.278 KB
  • CONCEPT_GENES gt=38 ms Completed: 38 ms rowSize= 23.020 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Deglutition Disorders C0011168
Definition (1)
Difficulty swallowing.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Esophageal Diseases C0014852
img Pharyngeal Diseases C0031345
Children (1)
img Esophageal Motility Disorders C0014858
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Gastrointestinal Diseases C00171784img Esophageal Diseases C0014852
img Stomatognathic Diseases C0038368img Pharyngeal Diseases C00313453img Pharyngeal Diseases C0031345
img Otorhinolaryngologic Diseases C0029896img Pharyngeal Diseases C00313453img Pharyngeal Diseases C0031345
Relationships (185)

Relation Types:
diso_​to_​anat : 22
diso_​to_​chem : 4
diso_​to_​diso : 154
diso_​to_​phys : 5


Relationships:
none : 91
associated_​with : 2
classifies : 1
disease_​may_​have_​finding : 50
isa : 10
location_​of : 1
mapped_​to : 25
parent_​is_​cdrh : 1
related_​to : 4
Page Size
Current 25
  Page 1 of 8
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHYS247img Deglutition C0011167
DISO_to_DISO163img Complication Aspects C1171258
DISO_to_DISO145img Cerebrovascular accident C0038454
DISO_to_DISO96img Esophageal Neoplasms C0014859
DISO_to_DISO95img Head and Neck Neoplasms C0018671
DISO_to_PHYS92img Deglutition C0011167
DISO_to_ANAT88img Esophagus C0014876
DISO_to_DISO83img Complication Aspects C1171258
DISO_to_DISO82img Cerebrovascular accident C0038454
DISO_to_DISO78img Esophageal Stenosis C0014866
DISO_to_DISO73img Esophageal Neoplasms C0014859
DISO_to_DISO68img COMPL POSTOP C0032787
DISO_to_ANAT61img Esophagus C0014876
DISO_to_DISO60img COMPL POSTOP C0032787
DISO_to_DISO58img Carcinoma, Squamous Cell C0007137
DISO_to_DISO56img Pneumonia, Aspiration C0032290
DISO_to_ANAT54img Cervical Vertebrae C0728985
DISO_to_ANAT54img Pharyngeal structure C0031354
DISO_to_DISO51img Aspiration Pneumonia C0032290
DISO_to_DISO50img Respiratory Aspiration C1720922
DISO_to_DISO48img Parkinson Disease C0030567
DISO_to_DISO45img Esophageal Stenosis C0014866
DISO_to_DISO45img Gastroesophageal Reflux C0017168
DISO_to_DISO42img Head and Neck Neoplasms C0018671
DISO_to_DISO40img Carcinoma, Squamous Cell C0007137
Genes (78)

Species:
human : 78
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanARX170302aristaless related homeobox
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanPANK280025pantothenate kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanWNK165125WNK lysine deficient protein kinase 1
INFERRED, Score=800, UMLKSK CUI: C0011168
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
img OMIM, Score=1000, UMLKSK CUI: C0011168
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanCHD755636chromodomain helicase DNA binding protein 7
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanPDP154704pyruvate dehyrogenase phosphatase catalytic subunit 1
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
INFERRED, Score=800, UMLKSK CUI: C0011168
HumanPNKD25953paroxysmal nonkinesigenic dyskinesia
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanNIPBL25836Nipped-B homolog (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0011168
HumanATXN1025814ataxin 10
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanNUP6223636nucleoporin 62kDa
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanVPS13A23230vacuolar protein sorting 13 homolog A (S. cerevisiae)
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanSETX23064senataxin
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanNPC210577Niemann-Pick disease, type C2
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
INFERRED, Score=800, UMLKSK CUI: C0011168
HumanCOLQ8292collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanPABPN18106poly(A) binding protein, nuclear 1
img OMIM, Score=1000, UMLKSK CUI: C0011168
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
INFERRED, Score=800, UMLKSK CUI: C0011168
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
INFERRED, Score=800, UMLKSK CUI: C0011168
HumanWFS17466Wolfram syndrome 1 (wolframin)
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanTSPYL17259TSPY-like 1
INFERRED, Score=800, UMLKSK CUI: C0011168
HumanTBP6908TATA box binding protein
img OMIM, Score=1000, UMLKSK CUI: C0011168
HumanCDKL56792cyclin-dependent kinase-like 5
img OMIM, Score=1000, UMLKSK CUI: C0011168
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011168Deglutition Disorders0self