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Details
Link-It Detail - Disease - Exophthalmos
Debug Stats
  • ### Total Build Time: 60 ms 37.511 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 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=4 ms Completed: 4 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 552 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.492 KB
  • CONCEPT_RELATIONSHIPS gt=32 ms Completed: 32 ms rowSize= 12.785 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 20.290 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Exophthalmos C0015300
Definition (1)
A protrusion of the eyeball from the socket.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Orbital Diseases C0029182
Children (1)
img Graves Disease C0018213
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C0015397img Orbital Diseases C00291823img Orbital Diseases C0029182
Relationships (56)

Relation Types:
diso_​to_​anat : 6
diso_​to_​diso : 49
diso_​to_​phen : 1


Relationships:
none : 38
classifies : 1
disease_​may_​have_​finding : 1
isa : 11
mapped_​to : 4
used_​for : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO34img Neoplasm of Orbit C0029185
DISO_to_ANAT33img Ocular orbit C0029180
DISO_to_ANAT31img Ocular orbit C0029180
DISO_to_DISO24img Neoplasm of Orbit C0029185
DISO_to_DISO22img Graves Disease C0018213
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_DISO16img Orbital Diseases C0029182
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_DISO13img Graves Ophthalmopathy C0339143
DISO_to_DISO13img Orbital Diseases C0029182
DISO_to_DISO11img C-C Fistula C0238045
DISO_to_DISO11img Diplopia C0012569
DISO_to_DISO9img A-760-766 DISORDERS OF THE EYELIDS C0015423
DISO_to_DISO8img Edema C0013604
DISO_to_DISO8img Graves Disease C0018213
DISO_to_ANAT7img Muscle of orbit C0028863
DISO_to_ANAT7img Sphenoid Bone C0037884
DISO_to_DISO7img 2-01 DISEASES OF THE NASAL SINUSES C0030469
DISO_to_DISO7img Adenocarcinoma C0001418
DISO_to_DISO7img Diplopia C0012569
DISO_to_DISO7img Meningioma C0025286
DISO_to_DISO7img Ophthalmoplegia C0029089
DISO_to_DISO7img Vision Disorders C0042790
DISO_to_DISO6img Graves Ophthalmopathy C0339143
DISO_to_DISO6img MUCOCELE C0026683
Genes (113)

Species:
human : 113
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRDX117189Graves disease, susceptibility to, X-linked
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanSCGB3A2117156secretoglobin, family 3A, member 2
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanFCRL3115352Fc receptor-like 3
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanLEPRE164175leucine proline-enriched proteoglycan (leprecan) 1
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanIFIH164135interferon induced with helicase C domain 1
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanFAM20C56975family with sequence similarity 20, member C
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanUACA55075uveal autoantigen with coiled-coil domains and ankyrin repeats
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanGRD250976Graves disease, susceptibility to, 2
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanSOST50964sclerostin
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanCD27429126CD274 molecule
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanPRDX525824peroxiredoxin 5
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanCXCR610663chemokine (C-X-C motif) receptor 6
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanCRTAP10491cartilage associated protein
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanPAX87849paired box 8
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanTNFRSF47293tumor necrosis factor receptor superfamily, member 4
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanTSHR7253thyroid stimulating hormone receptor
img OMIM, Score=1000, UMLKSK CUI: C0015300
HumanTPO7173thyroid peroxidase
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanTNFRSF1B7133tumor necrosis factor receptor superfamily, member 1B
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0015300
HumanTHY17070Thy-1 cell surface antigen
INFERRED, Score=800, UMLKSK CUI: C0015300
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015300Exophthalmos0self