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Details
Link-It Detail - Disease - Exotropia
Debug Stats
  • ### Total Build Time: 39 ms 32.073 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 524 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=4 ms Completed: 4 ms rowSize= 546 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 4.042 KB
  • CONCEPT_RELATIONSHIPS gt=15 ms Completed: 15 ms rowSize= 12.293 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 13.022 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Exotropia C0015310
Definition (1)
A form of ocular misalignment where the visual axes diverge inappropriately. For example, medial rectus muscle weakness may produce this condition as the affected eye will deviate laterally upon attempted forward gaze. An exotropia occurs due to the relatively unopposed force exerted on the eye by the lateral rectus muscle, which pulls the eye in an outward direction.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Strabismus C0038379
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Strabismus C0038379
img Nervous System Diseases C0027765img Cranial Nerve Diseases C00102665img Strabismus C0038379
img Eye Diseases C0015397img Ocular Motility Disorders C00288504img Strabismus C0038379
Relationships (30)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 23
diso_​to_​phys : 5


Relationships:
none : 13
classifies : 1
isa : 7
mapped_​to : 9
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT106img Muscle of orbit C0028863
DISO_to_ANAT58img Muscle of orbit C0028863
DISO_to_DISO53img Esotropia C0014877
DISO_to_DISO26img Esotropia C0014877
DISO_to_PHYS22img BV - Binocular vision C0042794
DISO_to_DISO20img COMPL POSTOP C0032787
DISO_to_DISO14img Complication Aspects C1171258
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_PHYS13img Convergence, Ocular C0009944
DISO_to_PHYS13img Eye Movements C0015413
DISO_to_PHYS11img Visual Acuity C0042812
DISO_to_DISO10img COMPL POSTOP C0032787
DISO_to_PHYS9img Accommodation, Ocular C0000936
DISO_to_DISOisaimg Alternating Exotropia C0152207
DISO_to_DISOmapped_toimg Congenital exotropia C1282374
DISO_to_DISOisaimg Consecutive exotropia C0339637
DISO_to_DISOmapped_toimg Distance exotropia C0730505
DISO_to_DISOmapped_toimg Divergent Strabismus C0015310
DISO_to_DISOisaimg Exotropia, Monocular C0152206
DISO_to_DISOmapped_toimg Exotropia, Primary C0339635
DISO_to_DISOisaimg Exotropia, Secondary C0339636
DISO_to_DISOmapped_toimg Incomitant exotropia C0423071
DISO_to_DISOisaimg Intermittent divergent squint C0423062
DISO_to_DISOmapped_toimg Manifest divergent squint C0423055
DISO_to_DISOmapped_toimg Near exotropia C0730506
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanBCOR54880BCL6 corepressor
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanGPR569289G protein-coupled receptor 56
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanTYR7299tyrosinase
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanTRPS17227trichorhinophalangeal syndrome I
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanTGFBR27048transforming growth factor, beta receptor II (70/80kDa)
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanTGFBR17046transforming growth factor, beta receptor 1
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanTBX16899T-box 1
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanSLC6A86535solute carrier family 6 (neurotransmitter transporter), member 8
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanEXT12131exostosin glycosyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanEFNB11947ephrin-B1
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanDPAGT11798dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanCOL4A11282collagen, type IV, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
img OMIM, Score=1000, UMLKSK CUI: C0015310
HumanACADSB36acyl-CoA dehydrogenase, short/branched chain
img OMIM, Score=1000, UMLKSK CUI: C0015310
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015310Exotropia0self