FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

770437002: Fundus pulverulentus (disorder)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3700860015 Fundus pulverulentus (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3700862011 Fundus pulverulentus en Synonym Active Case insensitive SNOMED CT core
3700861016 A rare form of patterned dystrophy of the retinal pigment epithelium characterized by a granular appearance in the macula, with coarse and punctiform mottling of the retinal pigment epithelium within the macular region. Association with choroidal neovascularization has been reported. en Definition Active Case sensitive SNOMED CT core
3700863018 A rare form of patterned dystrophy of the retinal pigment epithelium characterised by a granular appearance in the macula, with coarse and punctiform mottling of the retinal pigment epithelium within the macular region. Association with choroidal neovascularisation has been reported. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fundus pulverulentus Associated morphology Dystrophy true Inferred relationship Some 1
Fundus pulverulentus Is a Hereditary disorder of the visual system true Inferred relationship Some
Fundus pulverulentus Finding site Structure of retinal pigment epithelium true Inferred relationship Some 1
Fundus pulverulentus Is a Retinal pigment epithelial dystrophy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start