FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

1217640008: congenitale monoculaire elevatorverlamming van oog (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5036942016 Congenital monocular elevator palsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5036943014 Congenital monocular elevator palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
13590651000146115 congenitale monoculaire elevatorverlamming van oog nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13590661000146117 aangeboren 'elevator deficiency' in één oog nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13590671000146111 congenitale monoculaire elevatorverlamming van oog (aandoening) nl Fully specified name 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
Congenital monocular elevator palsy (disorder) Is a Congenital disease (disorder) false Inferred relationship Some
Congenital monocular elevator palsy (disorder) Is a Monocular elevator palsy (disorder) true Inferred relationship Some
Congenital monocular elevator palsy (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital monocular elevator palsy (disorder) Finding site Inferior rectus muscle structure (body structure) true Inferred relationship Some 1
Congenital monocular elevator palsy (disorder) Is a Congenital myopathy (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start