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29555009: Retinal disorder (disorder)

Status: current, 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
49448017 Retinal disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49451012 Retinal disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
760462019 Retinal disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303450013 Retinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
930771000195110 disturbo retinico it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
114651000087111 rétinopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
382111000241117 trouble rétinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50008101000188110 pathologie rétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
165321000274110 Retinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
651561000274118 Netzhauterkrankung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1383 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal disorder Is a Disorder of vitreous body and/or retina (disorder) true Inferred relationship Some
Retinal disorder Finding site Retinal structure true Inferred relationship Some 1
Retinal disorder Is a Chorioretinal disorder (disorder) false Inferred relationship Some
Retinal disorder Is a Retina finding (finding) false Inferred relationship Some
Retinal disorder Is a Retina finding (finding) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Retinal screening (procedure) Has focus True Retinal disorder Inferred relationship Some 2
Focal choroiditis of posterior pole of eye (disorder) Is a False Retinal disorder Inferred relationship Some
Retinal exudates and/or deposits Is a False Retinal disorder Inferred relationship Some
Retinal hemangioblastomatosis Is a False Retinal disorder Inferred relationship Some
Cerebroretinal microangiopathy with calcifications and cysts Is a True Retinal disorder Inferred relationship Some
Renal retinopathy Is a True Retinal disorder Inferred relationship Some
Hereditary vitreoretinopathy Is a True Retinal disorder Inferred relationship Some
Acute zonal occult outer retinopathy (AZOOR) is typified by acute loss of 1 or more zones of outer retinal function associated with photopsia, minimal funduscopic changes, and abnormal ERG findings Is a True Retinal disorder Inferred relationship Some
Retinopathy with acquired immunodeficiency syndrome (disorder) Is a True Retinal disorder Inferred relationship Some
Retinopathy due to unstable diabetes mellitus type 1 (disorder) Is a False Retinal disorder Inferred relationship Some
Retinopathy caused by canthaxanthin (disorder) Is a True Retinal disorder Inferred relationship Some
Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with retinal dystrophy. Is a True Retinal disorder Inferred relationship Some
A rare subtype of Joubert syndrome (JS) and related disorders (JSRD) characterised by the neurological features of JS associated with both renal and ocular disease. Is a True Retinal disorder Inferred relationship Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by severe global developmental delay, osteogenesis imperfecta, presence of wormian bones, seizures, ocular abnormalities (blue sclerae, optic atrophy, retinal detachment), and dysmorphic facial features (including frontal bossing, low anterior hairline, medial flare of the eyebrows, long eyelashes, hypertelorism, depressed nasal bridge, and low-set, large ears). There have been no further descriptions in the literature since 1994. Is a True Retinal disorder Inferred relationship Some
Background retinopathy due to impaired glucose regulation (disorder) Is a True Retinal disorder Inferred relationship Some
Revesz syndrome is a rare severe phenotypic variant of dyskeratosis congenita with an onset in early childhood, characterized by features of DC (e.g. skin hyper/hypopigmentation, nail dystrophy, oral leukoplakia, high risk of bone marrow failure (BMF) and cancer, developmental delay sparse and fine hair) in conjunction with bilateral exudative retinopathy, and intracranial calcifications. Is a True Retinal disorder Inferred relationship Some
Retinopathy of bilateral eyes (disorder) Is a False Retinal disorder Inferred relationship Some
Autoimmune retinopathy (disorder) Is a True Retinal disorder Inferred relationship Some
Proliferative retinopathy (disorder) Is a False Retinal disorder Inferred relationship Some
Hemorrhage of right retina (disorder) Is a False Retinal disorder Inferred relationship Some
Hemorrhage of left retina (disorder) Is a False Retinal disorder Inferred relationship Some
A rare, acquired retinal disorder characterized by unilateral, acute onset, rapidly progressive visual field loss. Sometimes patients have photopsia and complain of floaters. Typical ophthalmoscopic finding is a unilateral, yellowish-white annular intraretinal line, splitting the retinal field to affected outer retina with thinning, and normal retina. Gradual spontaneous visual recovery has been observed. Is a True Retinal disorder Inferred relationship Some
Retinal neovascularization due to occlusion of central retinal vein of left eye (disorder) Is a False Retinal disorder Inferred relationship Some
Retinal neovascularization due to occlusion of central retinal vein of right eye (disorder) Is a False Retinal disorder Inferred relationship Some
Retinal neovascularization due to occlusion of branch of retinal vein of left eye (disorder) Is a False Retinal disorder Inferred relationship Some
Retinal neovascularization due to occlusion of branch of retinal vein of right eye (disorder) Is a False Retinal disorder Inferred relationship Some
Toxic retinopathy (disorder) Is a True Retinal disorder Inferred relationship Some
Retinal light toxicity (disorder) Is a False Retinal disorder Inferred relationship Some
Purtscher's retinopathy Is a False Retinal disorder Inferred relationship Some
à l'examen : rétinopathie Is a False Retinal disorder Inferred relationship Some
No disease of retina of eye Associated finding True Retinal disorder Inferred relationship Some 1
Nerve fibre layer infarct Is a False Retinal disorder Inferred relationship Some
Retinopathy due to atherosclerosis (disorder) Is a True Retinal disorder Inferred relationship Some
Leukocoria Is a True Retinal disorder Inferred relationship Some
Chorioretinal disorder (disorder) Is a True Retinal disorder Inferred relationship Some
Lesion of retina Is a True Retinal disorder Inferred relationship Some
Disorder of retina of right eye (disorder) Is a True Retinal disorder Inferred relationship Some
Disorder of retina of left eye Is a True Retinal disorder Inferred relationship Some
Disorder of retina caused by talc (disorder) Is a True Retinal disorder Inferred relationship Some
Disorder of retina caused by radiation (disorder) Is a True Retinal disorder Inferred relationship Some

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