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Details
Link-It Detail - Disease - Orbital Diseases
Debug Stats
  • ### Total Build Time: 371 ms 37.673 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 213 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=10 ms Completed: 10 ms rowSize= 548 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 3.091 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.094 KB
  • CONCEPT_RELATIONSHIPS gt=77 ms Completed: 77 ms rowSize= 12.631 KB
  • CONCEPT_GENES gt=267 ms Completed: 267 ms rowSize= 18.431 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Orbital Diseases C0029182
Definition (1)
Diseases of the bony orbit and contents except the eyeball.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Eye Diseases C0015397
Children (7)
img Retrobulbar Hemorrhage C0302497
img Enophthalmos C0014306
img Exophthalmos C0015300
img Orbital Myositis C2350476
img Orbital Neoplasms C0029185
img Orbital Pseudotumor C0085270
img Orbital Cellulitis C0149507
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C00153972img Eye Diseases C0015397
Relationships (65)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 1
diso_​to_​diso : 58


Relationships:
none : 58
associated_​with : 1
classifies : 1
location_​of : 1
mapped_​to : 4
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO98img Cellulitis C0007642
DISO_to_DISO95img Complication Aspects C1171258
DISO_to_DISO90img Complication Aspects C1171258
DISO_to_DISO61img Abscess C0000833
DISO_to_ANAT51img Ocular orbit C0029180
DISO_to_DISO50img Paranasal Sinus Diseases C0030469
DISO_to_DISO39img Abscess C0000833
DISO_to_DISO39img Sinusitis C0037199
DISO_to_DISO38img Sinusitis C0037199
DISO_to_ANAT37img Ocular orbit C0029180
DISO_to_DISO34img 2-01 DISEASES OF THE NASAL SINUSES C0030469
DISO_to_DISO33img Cellulitis C0007642
DISO_to_DISO33img Mucormycosis C0026718
DISO_to_DISO32img Eyelid Diseases C0015423
DISO_to_DISO32img Mucormycosis C0026718
DISO_to_DISO31img A-760-766 DISORDERS OF THE EYELIDS C0015423
DISO_to_DISO30img Aspergillosis C0004030
DISO_to_DISO30img Graves Ophthalmopathy C0339143
DISO_to_DISO28img Pathological accumulation of air in tissues C0013990
DISO_to_DISO27img BACT EYE INFECT C0015404
DISO_to_DISO26img Cyst C0010709
DISO_to_DISO26img Eye Infections, Fungal C0015405
DISO_to_DISO25img chemically induced C0007994
DISO_to_DISO24img Cyst C0010709
DISO_to_DISO24img Wegener Granulomatosis C0043092
Genes (116)

Species:
human : 116
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRDX117189Graves disease, susceptibility to, X-linked
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanSCGB3A2117156secretoglobin, family 3A, member 2
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanFCRL3115352Fc receptor-like 3
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanLEPRE164175leucine proline-enriched proteoglycan (leprecan) 1
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanIFIH164135interferon induced with helicase C domain 1
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanUACA55075uveal autoantigen with coiled-coil domains and ankyrin repeats
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanGRD250976Graves disease, susceptibility to, 2
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanSOST50964sclerostin
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanCD27429126CD274 molecule
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanPRDX525824peroxiredoxin 5
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanCXCR610663chemokine (C-X-C motif) receptor 6
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanCRTAP10491cartilage associated protein
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanPAX87849paired box 8
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanTNFRSF47293tumor necrosis factor receptor superfamily, member 4
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanTSHR7253thyroid stimulating hormone receptor
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanTPO7173thyroid peroxidase
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanTNFRSF1B7133tumor necrosis factor receptor superfamily, member 1B
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0029182
HumanTHY17070Thy-1 cell surface antigen
img GENERIF, Score=734, Pubmed Id: 18976167, UMLKSK CUI: C0029182
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0029182Orbital Diseases0self