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Details
Link-It Detail - Disease - Endolymphatic Hydrops
Debug Stats
  • ### Total Build Time: 22 ms 15.240 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 415 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= 554 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 553 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.507 KB
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 7.188 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 3.361 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Endolymphatic Hydrops C0206586
Definition (1)
An accumulation of ENDOLYMPH in the inner ear (LABYRINTH) leading to buildup of pressure and distortion of intralabyrinthine structures, such as COCHLEA and SEMICIRCULAR CANALS. It is characterized by SENSORINEURAL HEARING LOSS; TINNITUS; and sometimes VERTIGO.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Labyrinth Diseases C0022890
Children (1)
img Meniere Disease C0025281
Ancestral Roots
RootRoot Plus OneDepthParent
img Otorhinolaryngologic Diseases C0029896img Ear Diseases C00134474img Labyrinth Diseases C0022890
Relationships (15)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 2
diso_​to_​diso : 8
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 12
isa : 1
permuted_​term_​of : 1
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO40img Auditory vertigo C0025281
DISO_to_DISO25img Auditory vertigo C0025281
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_DISO14img Complication Aspects C1171258
DISO_to_CHEM13img Contrast Media C0009924
DISO_to_CHEM13img Gadolinium DTPA C0060933
DISO_to_ANAT8img Cochlea C0009195
DISO_to_ANAT8img Ear, Inner C0022889
DISO_to_ANAT8img Endolymphatic Sac C0014168
DISO_to_DISO7img Hearing Loss, Sensorineural C0018784
DISO_to_PHEN7img genetic aspects C0017399
DISO_to_PHYS7img Otoacoustic Emission, Spontaneous C0162525
DISO_to_DISOused_forimg Auditory vertigo C0025281
DISO_to_DISOpermuted_term_ofimg Endolymphatic Hydrops C0206586
DISO_to_DISOisaimg Secondary endolymphatic hydrops C0456800
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanNAGA4668N-acetylgalactosaminidase, alpha-
INFERRED, Score=800, UMLKSK CUI: C0206586
HumanHLA-DRB13123
INFERRED, Score=800, UMLKSK CUI: C0206586
HumanAVPR2554arginine vasopressin receptor 2
INFERRED, Score=800, UMLKSK CUI: C0206586
HumanAVP551arginine vasopressin
INFERRED, Score=800, UMLKSK CUI: C0206586
HumanAQP2359aquaporin 2 (collecting duct)
INFERRED, Score=800, UMLKSK CUI: C0206586
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0206586Endolymphatic Hydrops0self