81745001: Structure of eye proper (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Body organ structure\Structure of sensory organ (body structure)\Eye structure

\Body system structure\Structure of special senses organ system\The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways\Eye region structure\Eye structure

\Body region structure\Structure of half of body lateral to midsagittal plane\Structure of half of head lateral to midsagittal plane\Eye region structure\Eye structure
\Body region structure\Body part structure\Upper body structure\Upper body part structure\Structure of head and/or neck (body structure)\Head structure (body structure)\Head part\Head region structure\Structure of half of head lateral to midsagittal plane\Eye region structure\Eye structure

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Eye structure	Is a	Body organ structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Eye structure	Is a	Orbital region structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Eye structure	partie de	Entire visual system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Eye structure	partie de	Entire orbital region	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Eye structure	Is a	Eye region structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Eye structure	partie de	Entire head	false	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Eye structure	Laterality	Side	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Eye structure	partie de	Entire visual system	false	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Eye structure	Is a	Structure of sensory organ (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Histoplasma capsulatum with retinitis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Ocular cryptococcosis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Progressive outer retinal necrosis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Parasitic endophthalmitis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Meningococcal eye disease (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Fungal infection of eye	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Cryptococcal endophthalmitis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Toxocara endophthalmitis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Ocular blastomycosis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Cytomegaloviral retinitis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Histoplasmosis with retinitis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Epstein-Barr virus infection of the retina	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Ocular toxoplasmosis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Herpes zoster retinitis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Measles keratoconjunctivitis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	5
uvéite liée à la reconstitution immunitaire	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Glaucoma caused by silicone oil	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
SOX2 anophthalmia syndrome (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Toxocara chorioretinitis (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Ocular toxocariasis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Parasitic eye infection (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ocular toxoplasmosis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Toxocara granuloma	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Colobomatous microphthalmia is a developmental disorder of the eye characterized by unilateral or bilateral microphthalmia associated with ocular coloboma.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Colobomatous microphthalmia is a developmental disorder of the eye characterized by unilateral or bilateral microphthalmia associated with ocular coloboma.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
A form of oculocutaneous albinism characterized by varying degrees of skin and hair hypopigmentation, numerous ocular changes and misrouting of the optic nerves at the chiasm.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Implantation of prosthetic intraocular lens (procedure)	Procedure site - Indirect (attribute)	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Secondary piggyback lens implantation (procedure)	Procedure site - Indirect (attribute)	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
insertion bilatérale d'une lentille intraoculaire prothétique	Procedure site - Indirect (attribute)	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Dyssegmental dysplasia with glaucoma syndrome	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare multiple congenital anomalies syndrome characterised by upper limb defects (hypoplastic thumb with hypoplasia of the metacarpal bone and phalanges and delayed bone maturation), developmental delay, central hearing loss, unilateral poorly developed antihelix, bilateral choroid coloboma and growth retardation.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
A rare multiple congenital anomalies syndrome characterised by upper limb defects (hypoplastic thumb with hypoplasia of the metacarpal bone and phalanges and delayed bone maturation), developmental delay, central hearing loss, unilateral poorly developed antihelix, bilateral choroid coloboma and growth retardation.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
CHIME syndrome is a rare ectodermal dysplasia syndrome characterised by ocular colobomas, cardiac defects, ichthyosiform dermatosis, intellectual disability, conductive hearing loss and epilepsy.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	10
Ophthalmic examination: no abnormality detected	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microcephaly - albinism - digital anomalies syndrome is a very rare syndrome associating microcephaly, micrognathia, oculocutaneous albinism, hypoplasia of the distal phalanx of fingers and agenesia of the distal end of the right big toe.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	8
Abruzzo Erickson syndrome	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Infection of eye caused by Avian Paramyxovirus 1 (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital oculocutaneous hypopigmentation	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Vici syndrome (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Glaucoma and sleep apnea syndrome	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A very rare congenital genetic neurological disorder characterised by agenesis/hypoplasia of corpus callosum with developmental abnormalities, ocular disorders, and variable craniofacial and skeletal abnormalities.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Intractable diarrhea with choanal atresia and eye anomaly syndrome	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	5
A rare syndrome of multiple congenital anomalies characterized by radial ray malformations, renal abnormalities (mild malrotation, ectopia, horseshoe kidney, renal hypoplasia, vesico-ureteral reflux, bladder diverticula), and ophthalmological abnormalities (mainly colobomas, but also microphthalmia, ptosis, and Duane anomaly). The phenotype overlaps with other SALL4-related disorders including Okihiro syndrome and Holt-Oram syndrome.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	5
A rare syndrome of multiple congenital anomalies characterized by radial ray malformations, renal abnormalities (mild malrotation, ectopia, horseshoe kidney, renal hypoplasia, vesico-ureteral reflux, bladder diverticula), and ophthalmological abnormalities (mainly colobomas, but also microphthalmia, ptosis, and Duane anomaly). The phenotype overlaps with other SALL4-related disorders including Okihiro syndrome and Holt-Oram syndrome.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Deaf blind hypopigmentation syndrome Yemenite type	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Microphthalmia with brain and digit anomaly	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Lowry MacLean syndrome (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Closed injury of eyeball (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Oculocerebrofacial syndrome Kaufman type	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Oculocutaneous albinism type 5 (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
A form of oculocutaneous albinism characterized by light hair at birth that darkens with age, white skin, transparent irides, photophobia, nystagmus, foveal hypoplasia and reduced visual acuity.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
A form of oculocutaneous albinism (OCA) characterised by skin and hair hypopigmentation (light blond to dark brown), nystagmus, iris transillumination, visual acuity ranging from 6/9 to 3/60 and hypopigmentation of the peripheral ocular fundus. Photophobia is not a major feature.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Ocular albinism with late-onset sensorineural deafness (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	6
A rare, genetic congenital malformation syndrome characterized by bilateral anophthalmia (or less commonly microphthalmia) in association with a variable combination of the following: pulmonary hypoplasia or agenesis, congenital diaphragmatic hernia or eventration, and variable cardiovascular defects (congenital heart defects and/or pulmonary artery atresia). Intellectual disability is noted in surviving patients. Other variable malformations affecting different organ systems, as well as facial dysmorphism, may be observed.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Penetrating wound of eyeball without foreign body (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Axial displacement of eyeball (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Prosthetic eye in situ (finding)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare multiple congenital anomalies/dysmorphic syndrome characterized by intellectual disability, severe visual impairment due to ocular malformations (microphthalmos and microcornea with sclerocornea), short stature, hypotrichosis, dental anomalies, and dysmorphic facial features (such as a narrow nasal bridge with marked distal flaring and low-set, protruding ears). There have been no further descriptions in the literature since 1992.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Duane anomaly, myopathy, scoliosis syndrome (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Ocular laceration without prolapse or loss of intraocular tissue	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare ectodermal dysplasia characterised by the association of epibulbar dermoids and aplasia cutis congenital.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
A rare primary glomerular disease characterized by the association of congenital nephrotic syndrome, early onset renal failure and ocular anomalies with microcoria and severe neurodevelopment deficits.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Colobomatous microphthalmia is a developmental disorder of the eye characterized by unilateral or bilateral microphthalmia associated with ocular coloboma.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A very rare congenital genetic neurological disorder characterised by agenesis/hypoplasia of corpus callosum with developmental abnormalities, ocular disorders, and variable craniofacial and skeletal abnormalities.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
CHIME syndrome is a rare ectodermal dysplasia syndrome characterised by ocular colobomas, cardiac defects, ichthyosiform dermatosis, intellectual disability, conductive hearing loss and epilepsy.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Demyelination of central nervous system co-occurrent and due to Sjogren disease (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Abruzzo Erickson syndrome	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spastic paraplegia, glaucoma, intellectual disability syndrome (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Deformity of eyeball	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Preaxial polydactyly, colobomata, intellectual disability syndrome	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudoprogeria syndrome	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Disorder due to insertion of glaucoma drainage device (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Disorder of eye co-occurrent and due to Marfan syndrome (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Disorder of eye caused by Toxoplasma gondii (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Eye appearance abnormal	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Eye sensation abnormal	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Renal coloboma syndrome (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Disorder of eye due to type 1 diabetes mellitus (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Binasal heteronymous quadrantanopia (finding)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Bitemporal heteronymous quadrantanopia	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pediatric onset Sjögren syndrome	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Repair of penetrating eye injury (procedure)	Procedure site - Direct (attribute)	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital trigeminal anesthesia (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Oculoauricular syndrome Schorderet type (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ophthalmic myiasis	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Colobomatous microphthalmia-rhizomelic dysplasia syndrome is a rare, genetic developmental defect during embryogenesis characterized by a range of developmental eye anomalies (including anophthalmia, microphthalmia, colobomas, microcornea, corectopia, cataract) and symmetric limb rhizomelia with short stature and contractures of large joints. Intellectual disability with autistic features, macrocephaly, dysmorphic features, urogenital anomalies (hypospadia, cryptorchidism), cutaneous syndactyly and precocious puberty may also be present.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Oculocutaneous albinism type 5 (disorder)	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A form of oculocutaneous albinism (OCA) characterised by skin and hair hypopigmentation (light blond to dark brown), nystagmus, iris transillumination, visual acuity ranging from 6/9 to 3/60 and hypopigmentation of the peripheral ocular fundus. Photophobia is not a major feature.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A form of oculocutaneous albinism characterized by light hair at birth that darkens with age, white skin, transparent irides, photophobia, nystagmus, foveal hypoplasia and reduced visual acuity.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Microcephaly - albinism - digital anomalies syndrome is a very rare syndrome associating microcephaly, micrognathia, oculocutaneous albinism, hypoplasia of the distal phalanx of fingers and agenesia of the distal end of the right big toe.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Oculocutaneous albinism type 1	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A form of oculocutaneous albinism characterized by varying degrees of skin and hair hypopigmentation, numerous ocular changes and misrouting of the optic nerves at the chiasm.	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Oculocutaneous albinism type 5 (disorder)	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A form of oculocutaneous albinism (OCA) characterised by skin and hair hypopigmentation (light blond to dark brown), nystagmus, iris transillumination, visual acuity ranging from 6/9 to 3/60 and hypopigmentation of the peripheral ocular fundus. Photophobia is not a major feature.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A form of oculocutaneous albinism characterized by light hair at birth that darkens with age, white skin, transparent irides, photophobia, nystagmus, foveal hypoplasia and reduced visual acuity.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microcephaly - albinism - digital anomalies syndrome is a very rare syndrome associating microcephaly, micrognathia, oculocutaneous albinism, hypoplasia of the distal phalanx of fingers and agenesia of the distal end of the right big toe.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Oculocutaneous albinism type 1	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A form of oculocutaneous albinism characterized by varying degrees of skin and hair hypopigmentation, numerous ocular changes and misrouting of the optic nerves at the chiasm.	Finding site	False	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
White forelock with malformations syndrome	Finding site	True	Eye structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4

Start Previous Page 47 of 50 Next End

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)

Back to Start

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
135599015	Eye	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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	Only initial character 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
823050013	Eye structure (body structure)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1204881015	Structure of eye proper (body structure)	en	Fully specified name	Active	Only initial character 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	Only initial character 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
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