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81745001: Structure of eye proper (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
135599015 Eye en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
135601018 Eyeball en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
504780011 Eye structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
504781010 Eyeball structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1204881015 Structure of eye proper (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2671957014 Structure of eye proper en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
274971000077119 structure de l'oeil fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
918961000172116 structure de l'œil fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
959291000172115 œil fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
995081000172116 oculus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
997961000172119 bulbe de l'œil fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1004911000172117 globe oculaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7023681000241115 structure de l'œil propre fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


943 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Eye structure Is a An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary). false Inferred relationship Some
Eye structure Is a Orbital region structure false Inferred relationship Some
Eye structure partie de Entire visual system false Inferred relationship Some
Eye structure partie de Entire orbital region false Inferred relationship Some
Eye structure Is a Eye region structure (body structure) true Inferred relationship Some
Eye structure partie de Entire head false Additional relationship Some
Eye structure Laterality Side (qualifier value) true Inferred relationship Some
Eye structure partie de Entire visual system false Additional relationship Some
Eye structure Is a Structure of sensory organ true Inferred relationship Some

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

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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