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Details
Link-It Detail - Disease - Laryngomalacia
Debug Stats
  • ### Total Build Time: 106 ms 18.794 KB
  • CONCEPT_NAME gt=9 ms Completed: 8 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 328 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=8 ms Completed: 8 ms rowSize= 1.404 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 7.979 KB
  • CONCEPT_RELATIONSHIPS gt=55 ms Completed: 55 ms rowSize= 5.036 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 2.369 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Laryngomalacia C0264303
Definition (1)
A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the LARYNX. This results in a floppy laryngeal wall making patency difficult to maintain.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Laryngeal Diseases C0023051
img Musculoskeletal Abnormalities C0151491
img Cartilage Diseases C0007302
Ancestral Roots
RootRoot Plus OneDepthParent
img Respiratory Tract Diseases C0035242img Laryngeal Diseases C00230513img Laryngeal Diseases C0023051
img Otorhinolaryngologic Diseases C0029896img Laryngeal Diseases C00230513img Laryngeal Diseases C0023051
img Musculoskeletal Diseases C0026857img Musculoskeletal Abnormalities C01514913img Musculoskeletal Abnormalities C0151491
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Musculoskeletal Abnormalities C0151491
img Musculoskeletal Diseases C0026857img Cartilage Diseases C00073023img Cartilage Diseases C0007302
img Skin and Connective Tissue Diseases C0175166img Connective Tissue Diseases C00097824img Cartilage Diseases C0007302
Relationships (10)

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


Relationships:
none : 4
is_​associated_​anatomic_​site_​of : 3
isa : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO12img Complication Aspects C1171258
DISO_to_ANAT8img Glottis C0017681
DISO_to_ANAT5img Epiglottis C0014540
DISO_to_DISO5img Gastroesophageal Reflux C0017168
DISO_to_ANATis_associated_anatomic_site_ofimg Head and neck structure C0460004
DISO_to_ANATis_associated_anatomic_site_ofimg Larynx C0023078
DISO_to_ANATis_associated_anatomic_site_ofimg Neck C0027530
DISO_to_DISOpermuted_term_ofimg Chondromalacia of Larynx C0264303
DISO_to_DISOisaimg Congenital laryngomalacia C0345160
DISO_to_DISOisaimg Laryngotracheomalacia C0585984
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanPOR5447P450 (cytochrome) oxidoreductase
img OMIM, Score=1000, UMLKSK CUI: C0264303
HumanEYA12138eyes absent homolog 1 (Drosophila)
img GENERIF, Score=1000, Pubmed Id: 16691597, UMLKSK CUI: C0264303
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0264303Laryngomalacia0self