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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:eye disease
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Accession:EFO:0003966 term browser browse the term
Definition:A non-neoplastic or neoplastic disorder that affects the eye. Representative examples include conjunctivitis, glaucoma, cataract, conjunctival squamous cell carcinoma, uveal melanoma, and retinoblastoma. A non-neoplastic or neoplastic disorder that affects the eye. Representative examples include conjunctivitis, glaucoma, cataract, conjunctival squamous cell carcinoma, uveal melanoma, and retinoblastoma. [NCIt:C26767] An eye and adnexa disease that is located in the eye.
Synonyms:exact_synonym: DOID:1242;   DOID:5614;   NCIT:C26767;   disease of eye;   disease of eyeball of camera-type eye;   disease or disorder of eyeball of camera-type eye;   disorder of eye;   disorder of eyeball of camera-type eye;   eye disorder;   eyeball of camera-type eye disease;   eyeball of camera-type eye disease or disorder;   globe disease;   http://identifiers.org/medgen/1370071;   http://identifiers.org/mesh/D005128;   http://identifiers.org/snomedct/371405004;   http://linkedlifedata.com/resource/umls/id/C4316870
 related_synonym: disease of eyeball;   disorder of eye proper;   disorder of eyeball;   disorder of globe
 xref: DOID:1242;   DOID:5614;   HP:0000478;   ICD10:H44;   ICD9:360;   ICD9:360.29;   ICD9:360.89;   ICD9:360.9;   ICD9:379.8;   ICD9:379.90;   MEDGEN:1370071;   MESH:D005128;   MONDO:0005328;   NCI:C26767;   SCTID:371405004;   UMLS:C0015397;   UMLS:C4316870;   Wikipedia:Eye_disease
 external_ontology: disease_has_location EFO:UBERON:0000019;   disease_has_location EFO:UBERON:0010230


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Term paths to the root
Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          disorder of visual system 0
            eye disease 0
              Accommodative esotropia 0
              Alagille syndrome + 0
              Axenfeld anomaly 0
              Ehlers-Danlos syndrome, kyphoscoliotic type 1 0
              Eye Injuries, Penetrating 0
              Foster-Kennedy syndrome 0
              GM1 gangliosidosis + 0
              Gardner syndrome 0
              Gaucher disease + 0
              Graves ophthalmopathy 0
              IRVAN syndrome 0
              IgG4-related ophthalmic disorder + 0
              Ito hypomelanosis 0
              LTBP2-related ocular dysgenesis + 0
              Lowry-MacLean syndrome 0
              Marshall syndrome 0
              Netherton syndrome 0
              Niemann-Pick disease type A 0
              Non-accomodative esotropia 0
              Opsoclonus-Myoclonus Syndrome 0
              Peters plus syndrome 0
              Rare genetic eye disease + 0
              Retrobulbar Hemorrhage 0
              Rothmund-Thomson syndrome type 2 0
              SHORT syndrome 0
              Smith-Lemli-Opitz syndrome 0
              Sturge-Weber syndrome 0
              Takayasu arteritis 0
              Tietz syndrome 0
              X-linked cone dysfunction syndrome with myopia 0
              alpha-mannosidosis + 0
              anterior segment dysgenesis + 0
              autoimmune/inflammatory optic neuropathy + 0
              blindness - scoliosis - arachnodactyly syndrome 0
              chondroectodermal dysplasia with night blindness 0
              choroidal neovascularization 0
              coloboma + 0
              conjunctival disorder + 0
              corneal disease + 0
              developmental defect of the eye + 0
              diabetic eye disease + 0
              dyssegmental dysplasia-glaucoma syndrome 0
              ectodermal dysplasia-blindness syndrome 0
              essential strabismus 0
              eye accommodation disease + 0
              eye adnexa disease + 0
              eye allergy + 0
              eye degenerative disorder + 0
              eye foreign body 0
              eye hemorrhage + 0
              eye infectious disorder + 0
              eye neoplasm + 0
              eyelid disease + 0
              familial cavitary optic disk anomaly 0
              fatty acyl-CoA reductase 1 deficiency 0
              galactosemia + 0
              galactosialidosis 0
              glaucoma + 0
              glaucoma-sleep apnea syndrome 0
              global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome 0
              hereditary hyperferritinemia with congenital cataracts 0
              hereditary optic neuropathy + 0
              isolated Pierre-Robin syndrome 0
              isolated ankyloblepharon filiforme adnatum 0
              isolated anophthalmia-microphthalmia syndrome + 0
              lacrimal apparatus disease + 0
              lamellar ichthyosis + 0
              lens disease + 0
              megalocornea-intellectual disability syndrome 0
              mevalonic aciduria 0
              microcornea-corectopia-macular hypoplasia syndrome 0
              microcornea-glaucoma-absent frontal sinuses syndrome 0
              microphthalmia + 0
              mucolipidosis type IV 0
              mucopolysaccharidosis type 1 + 0
              mucopolysaccharidosis type 6 + 0
              nail-patella syndrome 0
              neuroocular syndrome 0
              occular toxicity 0
              ocular cystinosis 0
              ocular hypertension 0
              ocular hypotension 0
              ocular motility disease + 0
              ocular motor apraxia, Cogan type 0
              ocular posterior capsular rupture 0
              ocular sarcoidosis 0
              ocular siderosis 0
              ocular vascular disease + 0
              oculocerebrorenal syndrome 0
              oculodentodigital dysplasia + 0
              oculomucocutaneous syndrome 0
              optic neuritis + 0
              phakomatosis pigmentovascularis + 0
              piebaldism 0
              pigment dispersion syndrome 0
              ptosis + 0
              red color blindness 0
              refractive error + 0
              retinopathy + 0
              rhizomelic chondrodysplasia punctata + 0
              scleral disorder + 0
              subacute myelo-opticoneuropathy 0
              syndromic recessive X-linked ichthyosis 0
              tyrosinemia type II 0
              uveal disorder + 0
              vitreous body disease + 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          head and neck disorder 0
            disease of orbital region 0
              eye disease 0
                Accommodative esotropia 0
                Alagille syndrome + 0
                Axenfeld anomaly 0
                Ehlers-Danlos syndrome, kyphoscoliotic type 1 0
                Eye Injuries, Penetrating 0
                Foster-Kennedy syndrome 0
                GM1 gangliosidosis + 0
                Gardner syndrome 0
                Gaucher disease + 0
                Graves ophthalmopathy 0
                IRVAN syndrome 0
                IgG4-related ophthalmic disorder + 0
                Ito hypomelanosis 0
                LTBP2-related ocular dysgenesis + 0
                Lowry-MacLean syndrome 0
                Marshall syndrome 0
                Netherton syndrome 0
                Niemann-Pick disease type A 0
                Non-accomodative esotropia 0
                Opsoclonus-Myoclonus Syndrome 0
                Peters plus syndrome 0
                Rare genetic eye disease + 0
                Retrobulbar Hemorrhage 0
                Rothmund-Thomson syndrome type 2 0
                SHORT syndrome 0
                Smith-Lemli-Opitz syndrome 0
                Sturge-Weber syndrome 0
                Takayasu arteritis 0
                Tietz syndrome 0
                X-linked cone dysfunction syndrome with myopia 0
                alpha-mannosidosis + 0
                anterior segment dysgenesis + 0
                autoimmune/inflammatory optic neuropathy + 0
                blindness - scoliosis - arachnodactyly syndrome 0
                chondroectodermal dysplasia with night blindness 0
                choroidal neovascularization 0
                coloboma + 0
                conjunctival disorder + 0
                corneal disease + 0
                developmental defect of the eye + 0
                diabetic eye disease + 0
                dyssegmental dysplasia-glaucoma syndrome 0
                ectodermal dysplasia-blindness syndrome 0
                essential strabismus 0
                eye accommodation disease + 0
                eye adnexa disease + 0
                eye allergy + 0
                eye degenerative disorder + 0
                eye foreign body 0
                eye hemorrhage + 0
                eye infectious disorder + 0
                eye neoplasm + 0
                eyelid disease + 0
                familial cavitary optic disk anomaly 0
                fatty acyl-CoA reductase 1 deficiency 0
                galactosemia + 0
                galactosialidosis 0
                glaucoma + 0
                glaucoma-sleep apnea syndrome 0
                global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome 0
                hereditary hyperferritinemia with congenital cataracts 0
                hereditary optic neuropathy + 0
                isolated Pierre-Robin syndrome 0
                isolated ankyloblepharon filiforme adnatum 0
                isolated anophthalmia-microphthalmia syndrome + 0
                lacrimal apparatus disease + 0
                lamellar ichthyosis + 0
                lens disease + 0
                megalocornea-intellectual disability syndrome 0
                mevalonic aciduria 0
                microcornea-corectopia-macular hypoplasia syndrome 0
                microcornea-glaucoma-absent frontal sinuses syndrome 0
                microphthalmia + 0
                mucolipidosis type IV 0
                mucopolysaccharidosis type 1 + 0
                mucopolysaccharidosis type 6 + 0
                nail-patella syndrome 0
                neuroocular syndrome 0
                occular toxicity 0
                ocular cystinosis 0
                ocular hypertension 0
                ocular hypotension 0
                ocular motility disease + 0
                ocular motor apraxia, Cogan type 0
                ocular posterior capsular rupture 0
                ocular sarcoidosis 0
                ocular siderosis 0
                ocular vascular disease + 0
                oculocerebrorenal syndrome 0
                oculodentodigital dysplasia + 0
                oculomucocutaneous syndrome 0
                optic neuritis + 0
                phakomatosis pigmentovascularis + 0
                piebaldism 0
                pigment dispersion syndrome 0
                ptosis + 0
                red color blindness 0
                refractive error + 0
                retinopathy + 0
                rhizomelic chondrodysplasia punctata + 0
                scleral disorder + 0
                subacute myelo-opticoneuropathy 0
                syndromic recessive X-linked ichthyosis 0
                tyrosinemia type II 0
                uveal disorder + 0
                vitreous body disease + 0
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