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Details
Link-It Detail - Disease - Eye Diseases
Debug Stats
  • ### Total Build Time: 140 ms 47.035 KB
  • CONCEPT_NAME gt=13 ms Completed: 13 ms rowSize= 367 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 282 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=13 ms Completed: 13 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 11.612 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=48 ms Completed: 48 ms rowSize= 14.435 KB
  • CONCEPT_GENES gt=59 ms Completed: 59 ms rowSize= 18.976 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 (2)
Eye Diseases C0015397
Disorder of eye
Definition (1)
Any deviation from the normal structure or function of the eye that is manifested by a characteristic set of symptoms and signs.
Semantic Types (1)
Disease or Syndrome (T047)
Children (27)
img Eye Neoplasms C0015414
img Eye Manifestations C0015411
img Lacrimal Apparatus Diseases C0022904
img Eye Abnormalities C0015393
img Retinal Diseases C0035309
img Refractive Errors C0034951
img Orbital Diseases C0029182
img Cogan Syndrome C0271270
img Eye Hemorrhage C0015402
img Ocular Hypertension C0028840
img Conjunctival Diseases C0009759
img Optic Nerve Diseases C0029132
img Corneal Diseases C0010034
img Eye Diseases, Hereditary C0015398
img Eye Infections C0015403
img Ocular Motility Disorders C0028850
img Eyelid Diseases C0015423
img Asthenopia C0004095
img Eye Injuries C0015408
img Ocular Hypotension C0028841
img Lens Diseases C0023308
img Vision Disorders C0042790
img Vitreoretinopathy, Proliferative C0242852
img Uveal Diseases C0042161
img Scleral Diseases C0036412
img Pupil Disorders C0034124
img Vitreous Detachment C0042907
Relationships (232)

Relation Types:
diso_​to_​anat : 24
diso_​to_​chem : 38
diso_​to_​diso : 157
diso_​to_​phen : 3
diso_​to_​phys : 10


Relationships:
none : 135
associated_​with : 2
classifies : 1
isa : 50
location_​of : 1
mapped_​to : 15
may_​diagnose : 3
may_​treat : 11
related_​to : 12
use : 2
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT211img Vitreous Body C0042905
DISO_to_ANAT199img Vitreous Body C0042905
DISO_to_DISO181img Complication Aspects C1171258
DISO_to_PHEN145img genetic aspects C0017399
DISO_to_DISO140img Complication Aspects C1171258
DISO_to_DISO120img chemically induced C0007994
DISO_to_ANAT98img Eye C0015392
DISO_to_DISO98img chemically induced C0007994
DISO_to_PHEN89img genetic aspects C0017399
DISO_to_DISO71img Vision Disorders C0042790
DISO_to_ANAT65img Eye C0015392
DISO_to_DISO60img Retinal Diseases C0035309
DISO_to_DISO58img Retinal Diseases C0035309
DISO_to_DISO55img Vision Disorders C0042790
DISO_to_PHYS55img Vision C0042789
DISO_to_PHYS45img Vision C0042789
DISO_to_DISO34img Sarcoidosis C0036202
DISO_to_ANAT31img Anterior Eye Segment C0003153
DISO_to_DISO30img COMPL POSTOP C0032787
DISO_to_DISO29img EYE INJ C0015408
DISO_to_DISO28img Dermatologic disorders C0037274
DISO_to_PHYS27img Visual Acuity C0042812
DISO_to_DISO26img Disease, Equine C0019940
DISO_to_DISO25img Blindness C0456909
DISO_to_ANAT24img Retina C0035298
Genes (1118)

Species:
human : 1118
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanCD24100133941CD24 molecule
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanRP33692221
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanMYP12664780myopia 12 (high grade, autosomal dominant)
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanSFTPA1653509surfactant protein A1
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanGDF6392255growth differentiation factor 6
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanARMS2387715age-related maculopathy susceptibility 2
img GENERIF, Score=673, Pubmed Id: 18423869, UMLKSK CUI: C0015397
HumanSUMO4387082small ubiquitin-like modifier 4
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanCERKL375298ceramide kinase-like
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanEYS346007eyes shut homolog (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanRD3343035retinal degeneration 3
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanVSX2338917visual system homeobox 2
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanCYP4V2285440cytochrome P450, family 4, subfamily V, polypeptide 2
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanTMEM114283953transmembrane protein 114
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanNPHP4261734nephronophthisis 4
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanMFSD8256471major facilitator superfamily domain containing 8
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanHYLS1219844hydrolethalus syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED, Score=800, UMLKSK CUI: C0015397
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0015397
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015397Eye Diseases0self