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424956000: Retinal pigment epithelial hyperplasia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2640868014 Retinal pigment epithelial hyperplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2644937018 Retinal pigment epithelial hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
2648772016 RPE hyperplasia en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypertrophy of retinal pigment epithelium Is a False Retinal pigment epithelial hyperplasia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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