723502001: Reticular dystrophy of retinal pigment epithelium (disorder)

\Degeneration of retina\Retinal dystrophy\...

\Retinal pigment epithelial dystrophy\Reticular dystrophy of retinal pigment epithelium (disorder)

\Hereditary retinal dystrophy\Reticular dystrophy of retinal pigment epithelium (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

3424856011 Reticular dystrophy of retinal pigment epithelium (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3424857019 Reticular dystrophy of retinal pigment epithelium en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core

1000841000172118 dystrophie réticulée de l'épithélium pigmentaire rétinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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

Inbound Relationships

Characteristic

Refinability

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
3424856011	Reticular dystrophy of retinal pigment epithelium (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3424857019	Reticular dystrophy of retinal pigment epithelium	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core
1000841000172118	dystrophie réticulée de l'épithélium pigmentaire rétinien	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module