FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

764939004: Fundus albipunctatus (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3655681014 Fundus albipunctatus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655682019 Fundus albipunctatus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404404017 Fundus albipunctatus is a rare, genetic retinal dystrophy disorder characterized by the presence of numerous small, round, yellowish-white retinal lesions that are distributed throughout the retina but spare the fovea. Patients present in childhood with non-progressive night blindness with prolonged cone and rod adaptation times. The macula may or may not be involved, which may result in a decrease of central visual acuity with age. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404405016 Fundus albipunctatus is a rare, genetic retinal dystrophy disorder characterised by the presence of numerous small, round, yellowish-white retinal lesions that are distributed throughout the retina but spare the fovea. Patients present in childhood with non-progressive night blindness with prolonged cone and rod adaptation times. The macula may or may not be involved, which may result in a decrease of central visual acuity with age. en Definition 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
Fundus albipunctatus Is a Autosomal hereditary disorder true Inferred relationship Some
Fundus albipunctatus Is a Hereditary retinal dystrophy true Inferred relationship Some
Fundus albipunctatus Is a Congenital disease (disorder) true Inferred relationship Some
Fundus albipunctatus Associated morphology Dystrophy true Inferred relationship Some 1
Fundus albipunctatus Occurrence Congenital true Inferred relationship Some 1
Fundus albipunctatus Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start