FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

1231661003: retinotopisch verstoorde oogvolgbewegingen (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5073742012 Retinotopic pursuit defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5073743019 Retinotopic pursuit defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
14730541000146110 retinotopisch verstoorde oogvolgbewegingen (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14730551000146113 retinotopisch verstoorde oogvolgbewegingen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinotopic pursuit defect Is a Deficiency of smooth pursuit movements true Inferred relationship Some
Retinotopic pursuit defect Finding site Structure of visual system (body structure) true Inferred relationship Some 1
Retinotopic pursuit defect Finding site Structure of nervous system (body structure) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start