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1217640008: Congenital monocular elevator palsy (disorder)


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
13817291000172117 congenitale monoculaire elevatorverlamming van oog nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
13817301000172116 aangeboren 'elevator deficiency' in één oog nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian 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) true 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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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