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95686007: Chorioretinal atrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
158512019 Chorioretinal atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839891013 Chorioretinal atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2324951000005112 Korioretinal atrofi da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chorioretinal atrophy Is a Disorder of choroid of eye false Inferred relationship Some
Chorioretinal atrophy Is a Retinal disorder false Inferred relationship Some
Chorioretinal atrophy Is a Chorioretinal disorder (disorder) false Inferred relationship Some
Chorioretinal atrophy Finding site Retinal structure false Inferred relationship Some 1
Chorioretinal atrophy Associated morphology Atrophy (morphologic abnormality) false Inferred relationship Some 1
Chorioretinal atrophy Finding site Choroidal structure false Inferred relationship Some 1
Chorioretinal atrophy Is a Degeneration of retina false Inferred relationship Some
Chorioretinal atrophy Is a Retina atrophic false Inferred relationship Some
Chorioretinal atrophy Is a Atrophic retina (disorder) true Inferred relationship Some
Chorioretinal atrophy Associated morphology Atrophy (morphologic abnormality) false Inferred relationship Some 1
Chorioretinal atrophy Finding site Retinal structure false Inferred relationship Some 1
Chorioretinal atrophy Finding site Choroidal structure false Inferred relationship Some 1
Chorioretinal atrophy Is a Choroidal atrophy true Inferred relationship Some
Chorioretinal atrophy Associated morphology Atrophy (morphologic abnormality) true Inferred relationship Some 2
Chorioretinal atrophy Finding site Choroidal structure true Inferred relationship Some 2
Chorioretinal atrophy Associated morphology Atrophy (morphologic abnormality) true Inferred relationship Some 3
Chorioretinal atrophy Finding site Retinal structure true Inferred relationship Some 3
Chorioretinal atrophy Is a Chorioretinal degeneration true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Gyrate atrophy of the choroid AND/OR retina (disorder) Is a False Chorioretinal atrophy Inferred relationship Some
Gyrate atrophy Is a True Chorioretinal atrophy Inferred relationship Some
Pigmented paravenous retinochoroidal atrophy (PPRCA) is a rare, commonly bilateral and symmetric retinal disease characterized by non-progressive or slowly progressive chorioretinal atrophy, peripapillary pigmentary changes and accumulation of bone-corpuscle pigmentation along the retinal veins and which is usually asymptomatic or can present with mild blurred vision. Is a True Chorioretinal atrophy Inferred relationship Some
Helicoid peripapillary chorioretinal degeneration is a rare autosomal dominantly inherited chorioretinal degeneration disease, presenting at birth or infancy, characterized by progressive bilateral retinal and choroidal atrophy, appearing as lesions on the optic nerve and peripheral ocular fundus and leading to central vision loss. Congenital anterior polar cataracts are sometimes associated with this disease. Is a True Chorioretinal atrophy Inferred relationship Some
A rare genetic developmental defect of the eye disease with characteristics of childhood onset of mild to severe myopia with microcornea and chorioretinal atrophy typically associated with telecanthus and posteriorly rotated ears. Other variable features include early-onset cataracts, ectopia lentis, ectopia pupil and retinal detachment. There is evidence the disease is caused by homozygous mutation in the ADAMTS18 gene on chromosome 16q23. Is a True Chorioretinal atrophy Inferred relationship Some
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. Is a True Chorioretinal atrophy Inferred relationship Some

This concept is not in any reference sets

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