5665001: Retinal structure (body structure)

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

\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).\Structure of sensory organ\Eye structure\Eye proper part (body structure)\...

\Eyeball segment structure\Posterior eyeball segment structure\Vitreous and/or retinal structures (body structure)\Retinal structure

\Structure of tunica interna of eyeball\Retinal 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 (body structure)\Eye structure\Eye proper part (body structure)\...

\Eyeball segment structure\Posterior eyeball segment structure\Vitreous and/or retinal structures (body structure)\Retinal structure

\Structure of tunica interna of eyeball\Retinal 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
Retinal structure	Is a	Structure of tunica interna of eyeball	true	Inferred relationship	Some
Retinal structure	Is a	Vitreous and/or retinal structures (body structure)	true	Inferred relationship	Some
Retinal structure	Is a	Choroidal and/or retinal structures	false	Inferred relationship	Some
Retinal structure	partie de	Entire tunica interna of eyeball	false	Additional relationship	Some
Retinal structure	partie de	Entire posterior segment of eyeball	false	Additional relationship	Some
Retinal structure	Laterality	Side (qualifier value)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital retinal dysplasia caused by teratogenic substance (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Chorioretinal rupture (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
High altitude retinopathy	Finding site	True	Retinal structure	Inferred relationship	Some	1
Stickler syndrome type 1	Finding site	True	Retinal structure	Inferred relationship	Some	4
Stickler syndrome type 2	Finding site	True	Retinal structure	Inferred relationship	Some	4
Stickler syndrome type 4 (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	4
Macular pseudohole	Finding site	True	Retinal structure	Inferred relationship	Some	2
Retinitis pigmentosa-deafness syndrome type 3 (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	4
Anterior proliferative vitreoretinopathy	Finding site	True	Retinal structure	Inferred relationship	Some	3
Posterior proliferative vitreoretinopathy	Finding site	True	Retinal structure	Inferred relationship	Some	3
Proliferative vitreoretinopathy	Finding site	True	Retinal structure	Inferred relationship	Some	3
Chorioretinal biopsy (procedure)	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1
Focal photocoagulation of chorioretinal lesion using laser (procedure)	Procedure site - Direct (attribute)	False	Retinal structure	Inferred relationship	Some	2
Grid photocoagulation of chorioretinal lesion using laser (procedure)	Procedure site - Direct (attribute)	False	Retinal structure	Inferred relationship	Some	2
Photodynamic therapy of chorioretinal lesion (procedure)	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1
Peripheral focal retinitis AND retinochoroiditis	Finding site	True	Retinal structure	Inferred relationship	Some	2
Focal juxtapapillary choroiditis	Finding site	False	Retinal structure	Inferred relationship	Some	2
Focal chorioretinal lesion	Finding site	True	Retinal structure	Inferred relationship	Some	1
Solitary raised chorioretinal lesion	Finding site	True	Retinal structure	Inferred relationship	Some	1
Multiple raised chorioretinal lesions	Finding site	True	Retinal structure	Inferred relationship	Some	1
Flat chorioretinal lesion	Finding site	True	Retinal structure	Inferred relationship	Some	1
Punched out chorioretinal lesion	Finding site	True	Retinal structure	Inferred relationship	Some	1
Diffuse chorioretinal lesion	Finding site	True	Retinal structure	Inferred relationship	Some	1
Focal chorioretinitis	Finding site	True	Retinal structure	Inferred relationship	Some	1
Retina and choroid finding	Finding site	True	Retinal structure	Inferred relationship	Some	1
Destruction of chorioretinal lesion	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1
Chorioretinal scar due to photocoagulation	Finding site	True	Retinal structure	Inferred relationship	Some	1
Chorioretinal disorder (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Chorioretinal neoplasm	Finding site	True	Retinal structure	Inferred relationship	Some	1
A rare, genetic, ophthalmic disorder characterized by the association of lens (ectopia and cataracts) and retinal (generalized tapetoretinal dystrophy and retinal detachment) anomalies, and variable myopia. Microcephaly and intellectual disability have been reported in some patients.	Finding site	True	Retinal structure	Inferred relationship	Some	1
Multifocal choroiditis and panuveitis syndrome (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Multifocal inner choroiditis	Finding site	False	Retinal structure	Inferred relationship	Some	3
Multifocal choroiditis and panuveitis syndrome (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	3
Multifocal choroiditis (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	3
Retinoschisis and retinal cysts	Finding site	True	Retinal structure	Inferred relationship	Some	3
Inflammation of retina due to chronic kidney disease stage 5	Finding site	True	Retinal structure	Inferred relationship	Some	1
A rare chromosomal anomaly syndrome, resulting from the partial deletion of the short arm of chromosome X, principally characterized by classical Norrie disease (bilateral, severe retinal malformations and opacity of the lens leading to congenital blindness, on occasion associated with progressive sensorineural deafness and intellectual disability), microcephaly, hypotonia, psychomotor and growth delay, moderate to severe mental handicap and disruptive behavior. Clinical phenotype is highly variable and immunodeficiency, epilepsy and hypogonadism have also been reported.	Finding site	True	Retinal structure	Inferred relationship	Some	3
X-linked intellectual disability-retinitis pigmentosa syndrome is characterized by moderate intellectual deficit and severe, early-onset retinitis pigmentosa. It has been described in five males spanning three generations of one family. Some patients also had microcephaly. It is transmitted as an X-linked recessive trait.	Finding site	True	Retinal structure	Inferred relationship	Some	3
Primary non-Hodgkin malignant lymphoma of vitreoretinal tract (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	2
Endolaser photocoagulation of retina	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1
Herpes simplex retinitis	Finding site	True	Retinal structure	Inferred relationship	Some	1
Intermediate uveitis caused by Borrelia burgdorferi (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	2
Repair of retina for retinal tear or defect by cryotherapy	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	2
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay with mild intellectual disability, short stature, facial dysmorphism (such as sparse hair, high forehead, deep-set eyes, short and upslanting palpebral fissures, short nose, anteverted nares, wide nasal base with broad nasal tip and broad columella, long philtrum, thin upper lip, and low-set, posteriorly rotated ears), and variable onset of sensorineural hearing loss and retinitis pigmentosa. Additional features are other ocular anomalies, abnormalities of the fingers, hypothyroidism, and signs of premature aging. Brain imaging shows cerebellar atrophy and dysmyelination.	Finding site	True	Retinal structure	Inferred relationship	Some	2
A rare, genetic retinal disorder characterized by bilateral iris coloboma, progressive retinal dystrophy and marked loss of vision, with or without congenital cataracts. Iridolenticular adhesions, scattered retinal pigmented epithelia mottling, and mild hypermetropic astigmatism may be associated.	Finding site	True	Retinal structure	Inferred relationship	Some	3
Rhegmatogenous retinal detachment with multiple breaks (disorder)	Finding site	False	Retinal structure	Inferred relationship	Some	2
New partial retinal detachment with multiple defects	Finding site	False	Retinal structure	Inferred relationship	Some	2
Tuberculous intermediate uveitis	Finding site	True	Retinal structure	Inferred relationship	Some	2
Bacterial panuveitis	Finding site	True	Retinal structure	Inferred relationship	Some	3
Syphilitic infectious intermediate uveitis	Finding site	True	Retinal structure	Inferred relationship	Some	1
Fungal panuveitis	Finding site	True	Retinal structure	Inferred relationship	Some	3
Retinal dystrophy due to GM2 gangliosidosis	Finding site	True	Retinal structure	Inferred relationship	Some	1
A rare hereditary ataxia characterised by neurogenic muscular atrophy associated with signs of cerebellar ataxia, hypaesthesia, degeneration of the retina, and diabetes mellitus. Onset of the disease is in adolescence and the course is slowly progressive. There have been no further descriptions in the literature since 1983.	Finding site	True	Retinal structure	Inferred relationship	Some	2
Hemangioblastoma of retina	Finding site	True	Retinal structure	Inferred relationship	Some	1
Reattachment of retina using endolaser photocoagulation	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1
Reattachment of retina using endolaser photocoagulation	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	2
A rare multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, choreoathetosis, progressive spastic diplegia, progressive tapetoretinal degeneration with loss of retinal vessels, and glomerulopathy resulting in death late in the first or early in the second decade of life. Absence of the cerebellar granular layer has been reported. There have been no further descriptions in the literature since 1982.	Finding site	True	Retinal structure	Inferred relationship	Some	2
Acute idiopathic enlarged blind spot syndrome	Finding site	True	Retinal structure	Inferred relationship	Some	3
Autoimmune retinitis (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
A rare, genetic, syndromic rod-cone dystrophy disorder characterized by psychomotor developmental delay from early childhood, intellectual disability, short stature, mild facial dysmorphism (e.g. upslanted palpebral fissures, hypoplastic alae nasi, malar hypoplasia, attached earlobes), excessive dental spacing and malocclusion, juvenile cataract and ophthalmologic findings of atypical retinitis pigmentosa (i.e. salt-and-pepper retinopathy, attenuated retinal arterioles, generalized rod-cone dysfunction, mottled macula, peripapillary sparing of retinal pigment epithelium).	Finding site	True	Retinal structure	Inferred relationship	Some	2
A rare, genetic, dermis elastic tissue disorder characterized by yellowish skin papules (resembling pseudoxanthoma elasticum) located on the neck, chest and/or flexural areas associated with loose, redundant, sagging skin on trunk and upper limbs, and retinitis pigmentosa, in the absence of clotting abnormalities. Patients present reduced night and peripheral vision, as well as optic nerve pallor, retinal pigment epithelium loss, attenuated retinal vessels and/or black pigment intra-retinal clumps.	Finding site	True	Retinal structure	Inferred relationship	Some	1
A rare congenital optic disc excavation characterised by deep fundus excavation of chorioretinal atrophy surrounding a relatively normal appearing optic disc. Retinal vasculature is normal, and retinochoroidal coloboma and glial anomalies are absent. Patients present with mostly unilateral markedly reduced visual acuity. Association with other congenital defects or systemic diseases is uncommon.	Finding site	True	Retinal structure	Inferred relationship	Some	3
Serpiginous choroiditis	Finding site	True	Retinal structure	Inferred relationship	Some	1
Multiple sclerosis associated intermediate uveitis	Finding site	True	Retinal structure	Inferred relationship	Some	2
Retinitis pigmentosa due to systemic disease	Finding site	True	Retinal structure	Inferred relationship	Some	1
Intermediate uveitis due to sarcoidosis	Finding site	True	Retinal structure	Inferred relationship	Some	2
Retinal implant in situ (finding)	Finding site	True	Retinal structure	Inferred relationship	Some	2
Retinal detachment due to degenerative progressive high myopia (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Tractional retinal detachment due to proliferative diabetic retinopathy (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Post-traumatic retinitis	Finding site	True	Retinal structure	Inferred relationship	Some	1
Disorder of retina due to sickle cell trait (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of slowly progressive night blindness, skeletal abnormalities (sloping shoulders, joint hyperextensibility, minor radiological anomalies) and characteristic facial features (periorbital anomalies, malar flatness, retrognathia). Additional manifestations include myopia and extinguished electroretinograms.	Finding site	True	Retinal structure	Inferred relationship	Some	4
Combined rhegmatogenous and tractional retinal detachment due to proliferative diabetic retinopathy (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Post-traumatic chorioretinopathy	Finding site	True	Retinal structure	Inferred relationship	Some	1
Retinoschisis - inner leaf break	Finding site	True	Retinal structure	Inferred relationship	Some	2
Retinoschisis - inner leaf break	Finding site	True	Retinal structure	Inferred relationship	Some	3
rétinoschisis par rupture du feuillet externe	Finding site	True	Retinal structure	Inferred relationship	Some	2
rétinoschisis par rupture du feuillet externe	Finding site	True	Retinal structure	Inferred relationship	Some	3
Primary malignant neuroepithelial neoplasm of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Break of retina with schisis of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Break of retina with schisis of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	2
Break of retina with schisis of retina (disorder)	Finding site	False	Retinal structure	Inferred relationship	Some	3
Multiple breaks of retina with schisis of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Multiple breaks of retina with schisis of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	2
Multiple breaks of retina with schisis of retina (disorder)	Finding site	False	Retinal structure	Inferred relationship	Some	3
Primary retinoblastoma of retina	Finding site	True	Retinal structure	Inferred relationship	Some	1
Usher syndrome type 1F (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Break of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Lesion of retina	Finding site	True	Retinal structure	Inferred relationship	Some	1
Multiple lesions of retina without detachment (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Multiple breaks of retina without detachment (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Detachment of retina with break of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Partial detachment of retina with single break of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
Partial detachment of retina with multiple breaks of retina (disorder)	Finding site	True	Retinal structure	Inferred relationship	Some	1
A rare primary bone dysplasia characterized by microcephaly, developmental delay and intellectual disability, sensorineural hearing loss, retinal degeneration, and skeletal dysplasia. Musculoskeletal abnormalities include delayed ossification of epiphyses, spondyloepimetaphyseal dysplasia, short stature, severe spinal deformities, and severe joint laxity resulting in multiple joint dislocations.	Finding site	True	Retinal structure	Inferred relationship	Some	1
Nonproliferative sickle cell retinopathy	Finding site	True	Retinal structure	Inferred relationship	Some	1
A disorder defined as retinal pigment disturbances including hypopigmentation and hyperpigmentation in colour fundus photographs that typically corresponded to hyperfluorescence and hypofluorescence in fluorescein angiogram images within or overlapping areas previously occupied by CNV (choroidal neovascularisation).	Finding site	True	Retinal structure	Inferred relationship	Some	2
A disorder defined as retinal pigment disturbances including hypopigmentation and hyperpigmentation in colour fundus photographs that typically corresponded to hyperfluorescence and hypofluorescence in fluorescein angiogram images within or overlapping areas previously occupied by CNV (choroidal neovascularisation).	Finding site	True	Retinal structure	Inferred relationship	Some	3
Retinopexy using diathermy	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1
Destruction of chorioretinal lesion by diathermy	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1
Repair of retinal tear	Procedure site - Direct (attribute)	True	Retinal structure	Inferred relationship	Some	1

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

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

US English

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Id	Description	Lang	Type	Status	Case?	Module
10443013	Retina	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
497668013	Retinal structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
795186017	Retinal structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
280141000077110	structure de la rétine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
878521000172117	retina	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
930631000172114	rétine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1013441000172110	structure rétinienne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module