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Details
Link-It Detail - Disease - Laryngostenosis
Debug Stats
  • ### Total Build Time: 123 ms 24.086 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 297 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=2 ms Completed: 2 ms rowSize= 305 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 1,004 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 5.423 KB
  • CONCEPT_RELATIONSHIPS gt=89 ms Completed: 89 ms rowSize= 12.610 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 2.979 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Laryngostenosis C0023075
Definition (1)
Developmental or acquired stricture or narrowing of the LARYNX. Symptoms of respiratory difficulty depend on the degree of laryngeal narrowing.
Semantic Types (3)
Congenital Abnormality (T019)
Acquired Abnormality (T020)
Disease or Syndrome (T047)
Parents (2)
img Respiratory System Abnormalities C0035238
img Laryngeal Diseases C0023051
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Respiratory System Abnormalities C0035238
img Respiratory Tract Diseases C0035242img Respiratory System Abnormalities C00352383img Respiratory System Abnormalities C0035238
img Respiratory Tract Diseases C0035242img Laryngeal Diseases C00230513img Laryngeal Diseases C0023051
img Otorhinolaryngologic Diseases C0029896img Laryngeal Diseases C00230513img Laryngeal Diseases C0023051
Relationships (29)

Relation Types:
diso_​to_​anat : 10
diso_​to_​diso : 19


Relationships:
none : 19
associated_​with : 1
classifies : 1
isa : 2
location_​of : 1
mapped_​to : 4
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO92img Tracheal Stenosis C0040583
DISO_to_DISO91img Tracheal Stenosis C0040583
DISO_to_DISO34img Complication Aspects C1171258
DISO_to_ANAT32img Trachea C0040578
DISO_to_DISO29img Complication Aspects C1171258
DISO_to_ANAT24img Cricoid Cartilage C0010323
DISO_to_ANAT23img Glottis C0017681
DISO_to_ANAT23img Larynx C0023078
DISO_to_ANAT22img Trachea C0040578
DISO_to_ANAT21img Cricoid Cartilage C0010323
DISO_to_ANAT18img Larynx C0023078
DISO_to_ANAT17img Glottis C0017681
DISO_to_DISO15img AIRWAY OBSTRUCTION C0001883
DISO_to_DISO13img AIRWAY OBSTRUCTION C0001883
DISO_to_DISO13img Wegener Granulomatosis C0043092
DISO_to_DISO11img COMPL POSTOP C0032787
DISO_to_DISO11img Laryngeal Neoplasms C0023055
DISO_to_ANAT10img Cartilage C0007301
DISO_to_DISO9img Laryngeal Neoplasms C0023055
DISO_to_ANATlocation_ofimg Larynx C0023078
DISO_to_DISOmapped_toimg Acquired Laryngeal Stenoses C0396052
DISO_to_DISOmapped_toimg Acquired Subglottic Stenoses C0340228
DISO_to_DISOassociated_withimg Acquired stenosis C0009814
DISO_to_DISOisaimg Congenital stenosis of larynx C0265758
DISO_to_DISOpermuted_term_ofimg Laryngostenosis C0023075
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img OMIM, Score=1000, UMLKSK CUI: C0023075
HumanFRAS180144Fraser syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0023075
HumanFLNB2317filamin B, beta
img OMIM, Score=1000, UMLKSK CUI: C0023075
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0023075Laryngostenosis0self