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Details
Link-It Detail - Disease - Hyperopia
Debug Stats
  • ### Total Build Time: 186 ms 32.870 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 502 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=2 ms Completed: 2 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=13 ms Completed: 13 ms rowSize= 553 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 1.494 KB
  • CONCEPT_RELATIONSHIPS gt=126 ms Completed: 126 ms rowSize= 12.384 KB
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 16.291 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperopia C0020490
Definition (1)
A refractive error in which rays of light entering the eye parallel to the optic axis are brought to a focus behind the retina, as a result of the eyeball being too short from front to back. It is also called farsightedness because the near point is more distant than it is in emmetropia with an equal amplitude of accommodation. (Dorland, 27th ed)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Refractive Errors C0034951
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C0015397img Refractive Errors C00349513img Refractive Errors C0034951
Relationships (33)

Relation Types:
diso_​to_​anat : 4
diso_​to_​diso : 25
diso_​to_​phys : 4


Relationships:
none : 19
classifies : 1
isa : 6
mapped_​to : 6
used_​for : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO183img Myopia C0027092
DISO_to_DISO122img Myopia C0027092
DISO_to_ANAT114img Cornea C0010031
DISO_to_ANAT67img Cornea C0010031
DISO_to_DISO57img Astigmatism C0004106
DISO_to_PHYS51img Refraction, Ocular C1261472
DISO_to_DISO49img ASTIGMATISM C0004106
DISO_to_DISO38img COMPL POSTOP C0032787
DISO_to_DISO36img Complication Aspects C1171258
DISO_to_PHYS32img Visual Acuity C0042812
DISO_to_PHYS28img Accommodation, Ocular C0000936
DISO_to_ANAT27img Corneal Stroma C0010040
DISO_to_DISO24img Amblyopia C0002418
DISO_to_ANAT23img Eye C0015392
DISO_to_DISO23img Complication Aspects C1171258
DISO_to_PHYS23img Accommodation, Ocular C0000936
DISO_to_DISO21img Anisometropia C0003081
DISO_to_DISO21img COMPL POSTOP C0032787
DISO_to_DISO21img Esotropia C0014877
DISO_to_DISOmapped_toimg Absolute hypermetropia C3266020
DISO_to_DISOisaimg Axial hypermetropia C0339675
DISO_to_DISOclassifiesimg Blindness and vision defects C0809996
DISO_to_DISOisaimg Curvature hypermetropia C0339676
DISO_to_DISOmapped_toimg Euhidrotic ectodermal dysplasia C1849805
DISO_to_DISOmapped_toimg Facultative hypermetropia C3266018
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanRDH12145226retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
img GENERIF, Score=861, Pubmed Id: 15322982, UMLKSK CUI: C0020490
HumanMFRP83552membrane frizzled-related protein
img GENERIF, Score=861, Pubmed Id: 15976030, UMLKSK CUI: C0020490
HumanNSD164324nuclear receptor binding SET domain protein 1
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanCRB123418crumbs homolog 1 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanKERA11081keratocan
img OMIM, Score=833, UMLKSK CUI: C0020490
HumanCLDN1610686claudin 16
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanNOG9241noggin
img GENERIF, Score=1000, Pubmed Id: 12089654, UMLKSK CUI: C0020490
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanKDM5C8242lysine (K)-specific demethylase 5C
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanTYR7299tyrosinase
img OMIM, Score=1000, UMLKSK CUI: C0020490
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanSLC6A86535solute carrier family 6 (neurotransmitter transporter), member 8
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanNDN4692necdin, melanoma antigen (MAGE) family member
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanMITF4286microphthalmia-associated transcription factor
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanFGD12245FYVE, RhoGEF and PH domain containing 1
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanERCC81161excision repair cross-complementing rodent repair deficiency, complementation group 8
img OMIM, Score=1000, UMLKSK CUI: C0020490
HumanFOXL2668forkhead box L2
img OMIM, Score=1000, UMLKSK CUI: C0020490
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020490Hyperopia0self