420535003: Peripapillary atrophy (finding)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Globe finding\Retina finding (finding)\Peripapillary atrophy (finding)

\Eye / vision finding\Globe finding\Retina finding (finding)\Peripapillary atrophy (finding)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2615715018 Peripapillary atrophy (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2618395015 Peripapillary atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2623177010 PPA - Peripapillary atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

5289141000241117 atrophie rétinienne péripapillaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

541901000274118 PPA - Peripapilläre Atrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

576361000274112 Peripapilläre Atrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Peripapillary atrophy (finding)	Is a	Retina finding (finding)	true	Inferred relationship	Some
Peripapillary atrophy (finding)	Associated morphology	Atrophy	false	Inferred relationship	Some	1
Peripapillary atrophy (finding)	Finding site	Peripapillary retina	false	Inferred relationship	Some	1
Peripapillary atrophy (finding)	Associated morphology	Atrophy	true	Inferred relationship	Some	1
Peripapillary atrophy (finding)	Finding site	Peripapillary retina	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
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	Peripapillary atrophy (finding)	Inferred relationship	Some

This concept is not in any reference sets