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ONTOLOGY REPORT - ANNOTATIONS


Term:hyperopia
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Accession:DOID:9834 term browser browse the term
Definition: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)
Synonyms:exact_synonym: far-sightedness;   farsightedness;   hypermetropia
 primary_id: MESH:D006956
 alt_id: RDO:0001058
 xref: ICD10CM:H52.0;   ICD9CM:367.0
For additional species annotation, visit the Alliance of Genome Resources.


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hyperopia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nog noggin JBrowse link 11 89,300,638 89,302,559 RGD:12801467
G Topors topoisomerase I binding, arginine/serine-rich JBrowse link 4 40,259,606 40,269,841 RGD:8554872
3MC syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Colec11 collectin sub-family member 11 JBrowse link 12 28,594,172 28,623,458 RGD:7240710
RGD:8554872
RGD:11554173
G Masp1 mannan-binding lectin serine peptidase 1 JBrowse link 16 23,451,785 23,521,240 RGD:11554173
Alazami-Yuan Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Taf6 TATA-box binding protein associated factor 6 JBrowse link 5 138,178,617 138,187,451 RGD:8554872
RGD:7240710
blepharophimosis, ptosis, and epicanthus inversus syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Copb2 coatomer protein complex, subunit beta 2 (beta prime) JBrowse link 9 98,563,731 98,588,375 RGD:8554872
G E330023G01Rik RIKEN cDNA E330023G01 gene JBrowse link 9 98,748,599 98,820,087 RGD:13592920
G Foxl2 forkhead box L2 JBrowse link 9 98,955,607 98,958,126 RGD:1598958
RGD:8554872
RGD:11554173
RGD:13592920
RGD:7240710
G Mrps22 mitochondrial ribosomal protein S22 JBrowse link 9 98,588,730 98,601,679 RGD:8554872
Duane retraction syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Chn1 chimerin 1 JBrowse link 2 73,610,660 73,775,367 RGD:8554872
RGD:11554173
G Mafb v-maf musculoaponeurotic fibrosarcoma oncogene family, protein B (avian) JBrowse link 2 160,363,677 160,367,065 RGD:13592920
RGD:11554173
G Sall4 spalt like transcription factor 4 JBrowse link 2 168,748,332 168,767,201 RGD:11556210
RGD:11554173
RGD:11532205
RGD:11556232
RGD:11556231
RGD:11556215
RGD:11556211
Duane Retraction Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mafb v-maf musculoaponeurotic fibrosarcoma oncogene family, protein B (avian) JBrowse link 2 160,363,677 160,367,065 RGD:8554872
Duane Retraction Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Chn1 chimerin 1 JBrowse link 2 73,610,660 73,775,367 RGD:8554872
RGD:7240710
Duane Retraction Syndrome 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mafb v-maf musculoaponeurotic fibrosarcoma oncogene family, protein B (avian) JBrowse link 2 160,363,677 160,367,065 RGD:8554872
RGD:7240710
esotropia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ankrd11 ankyrin repeat domain 11 JBrowse link 8 122,883,321 123,042,284 RGD:8554872
G Tfap2a transcription factor AP-2, alpha JBrowse link 13 40,713,802 40,738,238 RGD:8554872
high hyperopia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mfrp membrane frizzled-related protein JBrowse link 9 44,101,770 44,109,187 RGD:11076374
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sobp sine oculis binding protein JBrowse link 10 43,002,488 43,183,139 RGD:7240710
RGD:8554872
Nanophthalmos 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Myrf myelin regulatory factor JBrowse link 19 10,208,271 10,240,777 RGD:8554872
Nanophthalmos 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tmem98 transmembrane protein 98 JBrowse link 11 80,810,366 80,822,033 RGD:7240710
RGD:8554872
strabismus term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ahctf1 AT hook containing transcription factor 1 JBrowse link 1 179,744,904 179,804,015 RGD:8554872
G Bmp4 bone morphogenetic protein 4 JBrowse link 14 46,383,525 46,390,669 RGD:8699500
G Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit JBrowse link 8 84,338,631 84,640,251 RGD:8554872
G Foxp1 forkhead box P1 JBrowse link 6 98,925,342 99,522,746 RGD:8554872
G Gnb1 guanine nucleotide binding protein (G protein), beta 1 JBrowse link 4 155,491,300 155,559,269 RGD:8554872
G Kif7 kinesin family member 7 JBrowse link 7 79,698,098 79,715,772 RGD:8554872
G Med13l mediator complex subunit 13-like JBrowse link 5 118,560,330 118,765,438 RGD:8554872
G Nf1 neurofibromin 1 JBrowse link 11 79,339,590 79,581,609 RGD:8554872
G Pcdh19 protocadherin 19 JBrowse link X 133,582,860 133,689,044 RGD:8554872
G Sox5 SRY (sex determining region Y)-box 5 JBrowse link 6 143,828,425 144,782,287 RGD:8554872
G Stxbp1 syntaxin binding protein 1 JBrowse link 2 32,787,607 32,847,237 RGD:8554872
tarsal-carpal coalition syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nog noggin JBrowse link 11 89,300,638 89,302,559 RGD:7240710
RGD:8554872
RGD:12801450

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12767
    sensory system disease 4574
      eye disease 2301
        refractive error 171
          hyperopia 29
            Euhidrotic Ectodermal Dysplasia 0
            Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies 0
            Nanophthalmos 1 1
            Nanophthalmos 4 1
            high hyperopia 1
            strabismus + 24
            tarsal-carpal coalition syndrome 1
Path 2
Term Annotations click to browse term
  disease 12767
    disease of anatomical entity 12382
      nervous system disease 9893
        sensory system disease 4574
          eye disease 2301
            refractive error 171
              hyperopia 29
                Euhidrotic Ectodermal Dysplasia 0
                Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies 0
                Nanophthalmos 1 1
                Nanophthalmos 4 1
                high hyperopia 1
                strabismus + 24
                tarsal-carpal coalition syndrome 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.