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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal pigment epithelial hyperplasia (disorder) est un(e) (attribut) Retinal pigment epithelial abnormality true Inferred relationship Some
Retinal pigment epithelial hyperplasia (disorder) localisation d'une constatation (attribut) Structure of retinal pigment epithelium false Inferred relationship Some 1
Retinal pigment epithelial hyperplasia (disorder) morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 1
Retinal pigment epithelial hyperplasia (disorder) localisation d'une constatation (attribut) Structure of retinal pigment epithelium true Inferred relationship Some 1
Retinal pigment epithelial hyperplasia (disorder) morphologie associée (attribut) Hyperplasia (morphologic abnormality) true Inferred relationship Some 1

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

This concept is not in any reference sets

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