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Details
Link-It Detail - Disease - Retinal Diseases
Debug Stats
  • ### Total Build Time: 32 ms 46.025 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 330 bytes
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  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Retinal Diseases C0035309
Definition (1)

The retina is a layer of tissue in the back of your eye that senses light and sends images to your brain. In the center of this nerve tissue is the macula. It provides the sharp, central vision needed for reading, driving and seeing fine detail.

Retinal disorders affect this vital tissue. They can affect your vision, and some can be serious enough to cause blindness. Examples are

  • Retinal detachment - a medical emergency, when the retina is pulled away from the back of the eye
  • Macular pucker - scar tissue on the macula
  • Macular hole - a small break in the macula that usually happens to people over 60
  • Floaters - cobwebs or specks in your field of vision

NIH: National Eye Institute

Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Eye Diseases C0015397
Children (18)
img Retinal Perforations C0035321
img Retinal Detachment C0035305
img Retinal Vasculitis C0152026
img Diabetic Retinopathy C0011884
img Retinal Degeneration C0035304
img Retinitis C0035333
img Central Serous Chorioretinopathy C0730328
img Retinal Neovascularization C0035320
img Retinal Vein Occlusion C0035328
img Retinal Neoplasms C0524801
img Retinal Hemorrhage C0035317
img Retinal Artery Occlusion C0035302
img Leber Congenital Amaurosis C0339527
img Angioid Streaks C0002982
img Vitreoretinopathy, Proliferative C0242852
img Retinopathy of Prematurity C0035344
img Epiretinal Membrane C0339543
img Retinal Dysplasia C0035313
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C00153972img Eye Diseases C0015397
Relationships (233)

Relation Types:
diso_​to_​anat : 35
diso_​to_​chem : 29
diso_​to_​diso : 159
diso_​to_​phen : 4
diso_​to_​phys : 6


Relationships:
none : 140
associated_​with : 2
classifies : 2
is_​associated_​anatomic_​site_​of : 2
isa : 66
mapped_​to : 16
related_​to : 4
use : 1
Page Size
Current 25
  Page 1 of 10
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT362img Retina C0035298
DISO_to_ANAT254img Retina C0035298
DISO_to_DISO228img Complication Aspects C1171258
DISO_to_ANAT227img Retinal Vessels C0035330
DISO_to_PHEN224img genetic aspects C0017399
DISO_to_DISO214img chemically induced C0007994
DISO_to_DISO209img Complication Aspects C1171258
DISO_to_DISO188img CHOROID DIS C0008521
DISO_to_DISO185img chemically induced C0007994
DISO_to_ANAT173img Macula Lutea C0450295
DISO_to_PHEN169img genetic aspects C0017399
DISO_to_ANAT159img Retinal Vessels C0035330
DISO_to_DISO139img CHOROID DIS C0008521
DISO_to_ANAT118img Eye Pigment Epithelium C0031907
DISO_to_ANAT108img Vitreous Body C0042905
DISO_to_ANAT102img Macula Lutea C0450295
DISO_to_ANAT90img Vitreous Body C0042905
DISO_to_ANAT82img Retinal Pigment Epithelium C0035322
DISO_to_DISO76img Telangiectasis C0039446
DISO_to_ANAT75img Cell, Retinal Ganglion C0035316
DISO_to_CHEM74img ANGIOGENESIS INHIB C0596087
DISO_to_DISO74img Damage, Reperfusion C0035126
DISO_to_DISO68img Vision Disorders C0042790
DISO_to_CHEM66img Antibodies, Monoclonal C0003250
DISO_to_DISO61img Vision Disorders C0042790
Genes (490)

Species:
human : 490
Page Size
Current 25
  Page 1 of 20
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRP33692221
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanSFTPA1653509surfactant protein A1
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanSUMO4387082small ubiquitin-like modifier 4
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanCERKL375298ceramide kinase-like
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanEYS346007eyes shut homolog (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanCYP4V2285440cytochrome P450, family 4, subfamily V, polypeptide 2
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanNPHP4261734nephronophthisis 4
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanMFSD8256471major facilitator superfamily domain containing 8
img OMIM, Score=1000, UMLKSK CUI: C0035309
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanCLDN19149461claudin 19
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanRDH12145226retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanC8orf38137682
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanHIST3H2BB128312histone cluster 3, H2bb
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanLOC127086127086
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanHIST2H3C126961histone cluster 2, H3c
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanCPT1C126129carnitine palmitoyltransferase 1C
img GENERIF, Score=1000, Pubmed Id: 18385088, UMLKSK CUI: C0035309
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
img OMIM, Score=1000, UMLKSK CUI: C0035309
HumanSCGB3A192304secretoglobin, family 3A, member 1
INFERRED, Score=800, UMLKSK CUI: C0035309
HumanCDHR192211cadherin-related family member 1
img GENERIF, Score=1000, Pubmed Id: 16288196, UMLKSK CUI: C0035309
HumanTMEM6791147transmembrane protein 67
INFERRED, Score=800, UMLKSK CUI: C0035309
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0035309Retinal Diseases0self