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424956000: Retinal pigment epithelial hyperplasia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2640868014 Retinal pigment epithelial hyperplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2644937018 Retinal pigment epithelial hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2648772016 RPE hyperplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1376611000052118 hyperplasi av pigmentepitel i näthinna sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal pigment epithelial hyperplasia (disorder) Is a Retinal pigment epithelial abnormality true Inferred relationship Some
Retinal pigment epithelial hyperplasia (disorder) Finding site Structure of retinal pigment epithelium false Inferred relationship Some 1
Retinal pigment epithelial hyperplasia (disorder) Associated morphology Hyperplasia false Inferred relationship Some 1
Retinal pigment epithelial hyperplasia (disorder) Finding site Structure of retinal pigment epithelium true Inferred relationship Some 1
Retinal pigment epithelial hyperplasia (disorder) Associated morphology Hyperplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypertrophy of retinal pigment epithelium Is a False Retinal pigment epithelial hyperplasia (disorder) Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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