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Details
Link-It Detail - Disease - Diplopia
Debug Stats
  • ### Total Build Time: 26 ms 30.430 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 314 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 265 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=2 ms Completed: 2 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 4.061 KB
  • CONCEPT_RELATIONSHIPS gt=11 ms Completed: 11 ms rowSize= 12.604 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 11.299 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.143 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Diplopia C0012569
Definition (1)
The condition in which a single object appears as two objects. Also called "double vision." (from medterms.com)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Vision Disorders C0042790
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C0015397img Vision Disorders C00427903img Vision Disorders C0042790
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Vision Disorders C0042790
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Vision Disorders C0042790
Relationships (46)

Relation Types:
diso_​to_​anat : 4
diso_​to_​chem : 1
diso_​to_​diso : 39
diso_​to_​phys : 2


Relationships:
none : 36
classifies : 1
isa : 4
mapped_​to : 4
used_​for : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT46img Muscle of orbit C0028863
DISO_to_ANAT42img Muscle of orbit C0028863
DISO_to_DISO35img COMPL POSTOP C0032787
DISO_to_DISO34img Strabismus C0038379
DISO_to_DISO27img Strabismus C0038379
DISO_to_DISO22img chemically induced C0007994
DISO_to_DISO21img Orbital Fractures C0029184
DISO_to_DISO20img CRANIAL NERVE IV DIS C0702136
DISO_to_DISO17img CRANIAL NERVE IV DIS C0702136
DISO_to_DISO16img Abducens Nerve Diseases C0271355
DISO_to_DISO16img Blepharoptosis C0005745
DISO_to_DISO15img A-78 DISORDERS OF EYE MOVEMENTS C0028850
DISO_to_DISO15img Complication Aspects C1171258
DISO_to_DISO14img A-78 DISORDERS OF EYE MOVEMENTS C0028850
DISO_to_DISO14img COMPL POSTOP C0032787
DISO_to_DISO14img Graves Ophthalmopathy C0339143
DISO_to_DISO14img chemically induced C0007994
DISO_to_ANAT13img Ocular orbit C0029180
DISO_to_PHYS13img BV - Binocular vision C0042794
DISO_to_DISO12img Abducens Nerve Diseases C0271355
DISO_to_DISO11img Exophthalmos C0015300
DISO_to_DISO11img Oculomotor Nerve Diseases C0028866
DISO_to_DISO10img Myasthenia Gravis C0026896
DISO_to_DISO10img Orbital Fractures C0029184
DISO_to_ANAT9img Ocular orbit C0029180
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanCD24100133941CD24 molecule
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanTGFB17040transforming growth factor, beta 1
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanPTPRC5788protein tyrosine phosphatase, receptor type, C
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanSERPINI15274serpin peptidase inhibitor, clade I (neuroserpin), member 1
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanATXN34287ataxin 3
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanCIITA4261class II, major histocompatibility complex, transactivator
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanMAPT4137microtubule-associated protein tau
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanIL7R3575interleukin 7 receptor
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanHLA-DRB13123
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0012569
HumanCACNA1A773calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
img OMIM, Score=833, UMLKSK CUI: C0012569
HumanATP1A2477ATPase, Na+/K+ transporting, alpha 2 polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0012569
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0012569Diplopia0self