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Details
Link-It Detail - Disease - Nose Diseases
Debug Stats
  • ### Total Build Time: 45 ms 40.142 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 324 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 391 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= 1,009 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 4.363 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.014 KB
  • CONCEPT_RELATIONSHIPS gt=21 ms Completed: 21 ms rowSize= 12.765 KB
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 17.958 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Nose Diseases C0028432
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of the nose, which includes disorders which extend from the external structure, through the nasal cavity, sinuses and up to the nasopharynx.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Respiratory Tract Diseases C0035242
img Otorhinolaryngologic Diseases C0029896
Children (10)
img Choanal Atresia C0008297
img Nasal Polyps C0027430
img Nasal Obstruction C0027429
img Nose Neoplasms C0028433
img Paranasal Sinus Diseases C0030469
img Nose Deformities, Acquired C0028431
img Rhinoscleroma C0035468
img Granuloma, Lethal Midline C0018197
img Epistaxis C0014591
img Rhinitis C0035455
Ancestral Roots
RootRoot Plus OneDepthParent
img Respiratory Tract Diseases C00352422img Respiratory Tract Diseases C0035242
img Otorhinolaryngologic Diseases C00298962img Otorhinolaryngologic Diseases C0029896
Relationships (74)

Relation Types:
diso_​to_​anat : 8
diso_​to_​diso : 66


Relationships:
none : 42
associated_​with : 1
isa : 24
location_​of : 1
mapped_​to : 1
permuted_​term_​of : 1
related_​to : 4
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT64img Nasal Septum C0027432
DISO_to_DISO60img Complication Aspects C1171258
DISO_to_DISO52img 2-01 DISEASES OF THE NASAL SINUSES C0030469
DISO_to_DISO49img Complication Aspects C1171258
DISO_to_ANAT44img Nasal Septum C0027432
DISO_to_ANAT40img Nasal Cavity C0027423
DISO_to_DISO35img Fistula, Oral C0079943
DISO_to_DISO30img Mucormycosis C0026718
DISO_to_ANAT29img Nose C0028429
DISO_to_DISO28img COMPL POSTOP C0032787
DISO_to_DISO27img CANINE DIS C0012979
DISO_to_DISO25img Mucormycosis C0026718
DISO_to_DISO23img Brain Diseases C0006111
DISO_to_DISO22img 2-01 DISEASES OF THE NASAL SINUSES C0030469
DISO_to_DISO22img Fistula, Respiratory Tract C0080107
DISO_to_ANAT21img Nose C0028429
DISO_to_ANAT21img Surgical Flaps C0038925
DISO_to_DISO21img 755-756 HAMARTOMAS C0018552
DISO_to_DISO21img Cyst C0010709
DISO_to_DISO20img CANINE DIS C0012979
DISO_to_DISO20img chemically induced C0007994
DISO_to_DISO18img ASPERGILLOSIS C0004030
DISO_to_DISO18img Abscess C0000833
DISO_to_DISO17img Cyst, Nonodontogenic C0028309
DISO_to_DISO17img Fistula, Oral C0079943
Genes (171)

Species:
human : 171
Page Size
Current 25
  Page 1 of 7
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMUC5B727897mucin 5B, oligomeric mucus/gel-forming
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanCLEC4C170482C-type lectin domain family 4, member C
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanIL3390865interleukin 33
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanINHBE83729inhibin, beta E
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanP2RY1264805purinergic receptor P2Y, G-protein coupled, 12
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanTPSB264499tryptase beta 2 (gene/pseudogene)
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanIL22RA158985interleukin 22 receptor, alpha 1
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanSALL457167sal-like 4 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanLTB4R256413leukotriene B4 receptor 2
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanPHF1151131PHD finger protein 11
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanIL21R50615interleukin 21 receptor
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanCD20930835CD209 molecule
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanIL17B27190interleukin 17B
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanDNAI127019dynein, axonemal, intermediate chain 1
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanHAVCR126762hepatitis A virus cellular receptor 1
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanIL17RA23765interleukin 17 receptor A
INFERRED, Score=800, UMLKSK CUI: C0028432
HumanCLCA422802chloride channel accessory 4
INFERRED, Score=800, UMLKSK CUI: C0028432
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0028432Nose Diseases0self