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1186884006: aandoening van ruggenmerg door koperdeficiëntie (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4667902012 Myelopathy due to copper deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4668162013 Disorder of spinal cord due to copper deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4668163015 Disorder of spinal cord due to copper deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
13270181000146116 aandoening van ruggenmerg door koperdeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13270191000146119 myelopathie door koperdeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13270201000146117 aandoening van ruggenmerg door koperdeficiëntie (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
Myelopathy due to copper deficiency Is a Myelopathy due to nutritional deficiency (disorder) true Inferred relationship Some
Myelopathy due to copper deficiency Due to Hypocupremia true Inferred relationship Some 2
Myelopathy due to copper deficiency Finding site Spinal cord 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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