Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Glaucoma of childhood |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary childhood glaucoma following congenital cataract surgery |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Angle closure glaucoma suspect (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Glaucoma suspect caused by corticosteroid |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Glaucoma suspect due to diabetes mellitus type 2 (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Open angle glaucoma suspect (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Glaucoma due to congenital anomaly of eye |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Glaucoma due to Lowe syndrome |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Congenital glaucoma |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Primary congenital glaucoma (disorder) |
Finding site |
False |
Eye structure |
Inferred relationship |
Some |
2 |
Spastic paraplegia-glaucoma-intellectual disability syndrome is characterized by progressive spastic paraplegia, glaucoma and intellectual deficit. It has been described in two families. The second described sibship was born to consanguineous parents. The mode of inheritance is autosomal recessive. |
Finding site |
False |
Eye structure |
Inferred relationship |
Some |
2 |
Bilateral primary congenital glaucoma |
Finding site |
False |
Eye structure |
Inferred relationship |
Some |
4 |
Luxation of eye |
Finding site |
False |
Eye structure |
Inferred relationship |
Some |
3 |
Secondary syphilis of eye (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Glaucoma due to and following traumatic injury of globe of eye (disorder) |
Finding site |
False |
Eye structure |
Inferred relationship |
Some |
1 |
Primary glaucoma due to combination of mechanisms |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Sticky sensation of eye (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Prosthetic eye in situ (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Behcet disease of eye |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Reinsertion of implant of eyeball with conjunctival graft |
Procedure site - Indirect (attribute) |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Histologic type of primary malignant neoplasm of eye |
This attribute specifies the location of the entity specified by the attribute "Inheres in". |
False |
Eye structure |
Inferred relationship |
Some |
5 |
Small incision phacoemulsification of cataract and insertion of intraocular lens |
Procedure site - Indirect (attribute) |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Phacoemulsification of cataract with intraocular lens implantation (procedure) |
Procedure site - Indirect (attribute) |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Bimanual phacoemulsification of cataract with intraocular lens implantation (procedure) |
Procedure site - Indirect (attribute) |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Bimanual microincisional phacoemulsification of cataract with intraocular lens implantation (procedure) |
Procedure site - Indirect (attribute) |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Anatomic location directly invaded by primary malignant neoplasm of eye (observable entity) |
This attribute specifies the location of the entity specified by the attribute "Inheres in". |
False |
Eye structure |
Inferred relationship |
Some |
6 |
Contact lens related red eye |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Postoperative emulsification of silicone oil in eye |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Presence of primary malignant neoplasm of eye at surgical margin in excised tissue specimen (observable entity) |
This attribute specifies the location of the entity specified by the attribute "Inheres in". |
False |
Eye structure |
Inferred relationship |
Some |
7 |
Surgical margin involved by primary malignant neoplasm of eye in excised tissue specimen |
This attribute specifies the location of the entity specified by the attribute "Inheres in". |
False |
Eye structure |
Inferred relationship |
Some |
7 |
Eye disease caused by Adenovirus (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Invasive ocular aspergillosis |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Intraocular non-Hodgkin malignant lymphoma (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Deep sclerectomy (procedure) |
Procedure site |
False |
Eye structure |
Inferred relationship |
Some |
3 |
Silicone oil in eye following vitrectomy (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary lens implant |
Procedure site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Primary piggyback lens implantation (procedure) |
Procedure site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary piggyback lens implantation (procedure) |
Procedure site |
True |
Eye structure |
Inferred relationship |
Some |
3 |
Presbyopic refractive lensectomy with intraocular lens implantation |
Procedure site |
False |
Eye structure |
Inferred relationship |
Some |
3 |
Refractive lensectomy with intraocular lens implantation (procedure) |
Procedure site |
False |
Eye structure |
Inferred relationship |
Some |
3 |
One stage extracapsular extraction of lens and insertion of prosthetic intraocular lens by inferior temporal route (procedure) |
Procedure site |
False |
Eye structure |
Inferred relationship |
Some |
3 |
One stage intracapsular extraction of lens by inferior temporal route and insertion of prosthetic intraocular lens (procedure) |
Procedure site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
One stage intracapsular extraction of lens with insertion of prosthetic intraocular lens (procedure) |
Procedure site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
One stage extracapsular extraction of lens and insertion of prosthetic intraocular lens (procedure) |
Procedure site |
False |
Eye structure |
Inferred relationship |
Some |
2 |
insertion bilatérale d'une lentille intraoculaire prothétique |
Procedure site |
False |
Eye structure |
Inferred relationship |
Some |
3 |
Spastic paraplegia-glaucoma-intellectual disability syndrome is characterized by progressive spastic paraplegia, glaucoma and intellectual deficit. It has been described in two families. The second described sibship was born to consanguineous parents. The mode of inheritance is autosomal recessive. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Cataract fragments in the eye post cataract surgery (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Epibulbar lipodermoid - preauricular appendages - polythelia is a branchial arch syndrome described in seven sibs of one Danish family and characterized by supernumerary nipples (polythelia), preauricular appendages and often binocular epibulbar lipodermoids or unilateral subconjunctival lipodermoids. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Acquired anophthalmic socket with orbital implant |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Congenital colobomatous cyst of orbit (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Complex displacement of eyeball |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Atrophy of globe of eye |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Phthisis bulbi |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
A rare neurologic disease characterized by the presence of Duane retraction syndrome (a congenital cranial dysinnervation disorder with unilateral or bilateral limitation of abduction and/or adduction of the eye, as well as globe retraction and palpebral fissure narrowing on attempted adduction) in combination with congenital unilateral or bilateral hearing loss. The sidedness of hearing loss corresponds to the sidedness of the retraction syndrome. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Intraocular medulloepithelioma is a rare eye tumor characterized by a white, gray or yellow-colored cystic mass that arises from the primitive neuroectodermal, nonpigmented epithelium of the ciliary body, or occasionally from the optic nerve, optic disc, retina or iris. Typically it has a benign clinical course with good prognosis and generally presents with childhood onset of poor vision and pain, glaucoma, and/or cataract. Leukocoria, exotropia, exophthalmos, strabismus, epiphora, change in eye color, hyphema, and raised intraocular pressure are also remarkable manifestations. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Glaucoma following ocular onchocerciasis (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Glaucoma due to and following retinopathy of prematurity (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Perforating injury of eyeball (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Traumatic entrapment of eyeball |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
High pressure primary open-angle glaucoma |
Finding site |
False |
Eye structure |
Inferred relationship |
Some |
1 |
Downward displacement of eyeball (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Medial displacement of eye (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Upward displacement of eyeball (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Primary oculocerebral lymphoma is a rare, primary, organ-specific, extranodal non-Hodgkin's lymphoma (typically diffuse large B-cell lymphoma), simultaneously affecting the intraocular compartments (retina, vitreous, optic nerve, uvea and others) and the central nervous system (commonly the cerebellum, spinal cord or pia mater). The presenting symptoms vary depending on the localization of the tumor and may include vitreous floaters or blurred vision, raised intracranial pressure (headache, vomiting, papilledema) and/or focal neurological deficits. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Ocular fistula causing hypotony of eye |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
A subtype of Waardenburg syndrome (WS) with characteristics of congenital deafness, minor defects in structures arising from neural crest resulting in pigmentation anomalies of eyes, hair, and skin, in combination with dystopia canthorum. Caused by a heterozygous mutation in the paired box-containing PAX3 gene on chromosome 2q36.1. In the majority of cases, WS1 is transmitted as an autosomal dominant disorder with a large variable inter and intrafamilial expressivity. Some affected patients present with a de novo mutation. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
5 |
An autosomal dominant subtype of Waardenburg syndrome (WS) with characteristics of varying degrees of deafness and pigmentation anomalies of eyes, hair and skin but without dystopia canthorum. The disease is genetically very heterogeneous, mutations have been found in MITF (3p14-p13; subtype designated as WS2A), SNAI2 (8q11.21; WS2D), and SOX10 (22q13.1; WS2E) genes. Furthermore WS2 loci have been mapped to chromosome 1p21-p13.3 (subtype designated as WS2B) and to chromosome 8p23 (designated as WS2C). Digenic inheritance of MITF mutation in combination a TYR mutation (and/or the TYRR402Q hypomorphic allele) has been reported in two families with WS2 and ocular albinism. In the majority of cases, WS2 is transmitted as an autosomal dominant disorder with a large variable inter and intrafamilial expressivity. Some affected patients present with a de novo mutation. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Neovascularization of eye due to hemispheric retinal vein occlusion |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Neovascularization of eye due to juvenile central retinal vein occlusion |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Irrigation of eye |
Procedure site - Direct (attribute) |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Primary malignant glioma of eye |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Neonatal ophthalmologic disorder (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Immature eyes (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Scleral reinforcement surgery balloon catheter |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Eye structure |
Inferred relationship |
Some |
|
A rare genetic disease characterized by a highly variable phenotype comprising ocular anomalies (congenital glaucoma, myopia, retinal detachment, and/or Axenfeld-Rieger anomaly), congenital hypothyroidism, hearing loss, microcephaly, dental defects, kidney anomalies, cerebrovascular anomalies, and distal limb anomalies. Dysmorphic facial features may include square face with prominent jaw, broad flat nasal bridge, short philtrum, and prominent ears. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Steroid-induced glaucoma glaucomatous stage |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Open angle glaucoma caused by corticosteroid (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Target intraocular pressure |
This attribute specifies the independent continuant which bears the quality, and on which the dependent quality (of this observable) depends. |
False |
Eye structure |
Inferred relationship |
Some |
2 |
Pain on movement of eye (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
A rare developmental defect during embryogenesis characterized by unilateral duplication of an eye which may appear as a synophthalmic eye in a single orbit or as two separate unilateral eyes, each in a separate orbit. The malformation is always associated with other anomalies of the central nervous system (such as porencephaly, meningocele, or arachnoidal cysts) and with craniofacial abnormalities. A proboscis is often found. Clinically, moderate mental retardation and epilepsy are typical. |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Primary ocular hypertension |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary ocular hypertension due to uveitis |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary ocular hypertension |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary ocular hypertension due to pseudoexfoliation |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary ocular hypertension due to aphakia |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Ocular hypertension due to neovascularization (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary ocular hypertension due to pigment dispersion syndrome |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Secondary ocular hypertension due to ocular trauma |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Ocular hypertension caused by corticosteroid (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Neovascularization of eye (finding) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Traumatic injury of globe of eye (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Intraocular pressure |
This attribute specifies the independent continuant which bears the quality, and on which the dependent quality (of this observable) depends. |
False |
Eye structure |
Inferred relationship |
Some |
2 |
The highest recorded or patient reported intraocular pressure as documented before any treatment was administered. |
This attribute specifies the independent continuant which bears the quality, and on which the dependent quality (of this observable) depends. |
False |
Eye structure |
Inferred relationship |
Some |
2 |
The maximum intraocular pressure as documented in the patient's previous records or reported by the patient. |
This attribute specifies the independent continuant which bears the quality, and on which the dependent quality (of this observable) depends. |
False |
Eye structure |
Inferred relationship |
Some |
2 |
Ocular hypertension due to angle recession |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Ocular hypertension due to ocular surgery (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
3 |
Open angle glaucoma caused by drug (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Ocular hypertension due to intraocular neoplasm (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Ocular hypertension due to ocular vascular disorder (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |
Ocular hypertension caused by silicone oil |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
1 |
Ocular hypertension due to intraocular hemorrhage (disorder) |
Finding site |
True |
Eye structure |
Inferred relationship |
Some |
2 |