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723502001: Reticular dystrophy of retinal pigment epithelium (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3424856011 Reticular dystrophy of retinal pigment epithelium (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3424857019 Reticular dystrophy of retinal pigment epithelium en Synonym Active Case insensitive SNOMED CT core
3424858012 A patterned dystrophy of the retinal pigment epithelium with a progressive course. The disease is characterized by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. Sometimes associated with scleral staphyloma, choroidal neovascularization, convergent strabismus, spherophakia with myopia and luxated lenses and partial atrophy of the iris. en Definition Active Case sensitive SNOMED CT core
3424859016 A patterned dystrophy of the retinal pigment epithelium with a progressive course. The disease is characterised by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. Sometimes associated with scleral staphyloma, choroidal neovascularisation, convergent strabismus, spherophakia with myopia and luxated lenses and partial atrophy of the iris. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Reticular dystrophy of retinal pigment epithelium Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Reticular dystrophy of retinal pigment epithelium Is a Hereditary retinal dystrophy true Inferred relationship Some
Reticular dystrophy of retinal pigment epithelium Is a Retinal pigment epithelial dystrophy true Inferred relationship Some
Reticular dystrophy of retinal pigment epithelium Associated morphology Dystrophy true Inferred relationship Some 1
Reticular dystrophy of retinal pigment epithelium Finding site Structure of retinal pigment epithelium true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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