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41574007: Paramyotonia congenita (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
69350017 Paramyotonia congenita en Synonym Active Entire term case insensitive SNOMED CT core module
69351018 Eulenburg syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
778377012 Paramyotonia congenita (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1229775013 Eulenburg's disease en Synonym Active Entire term case sensitive SNOMED CT core module
1229776014 Eulenburg disease en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Paramyotonia congenita Is a Myotonic disorder true Inferred relationship Existential restriction modifier
Paramyotonia congenita Is a Myopathy false Inferred relationship Existential restriction modifier
Paramyotonia congenita Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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