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41574007: Paramyotonia congenita (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
69350017 Paramyotonia congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
69351018 Eulenburg syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
778377012 Paramyotonia congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229775013 Eulenburg's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1229776014 Eulenburg disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
69350017 Paramyotonia congenita en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
69350017 Paramyotonia congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
69351018 Eulenburg syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
778377012 Paramyotonia congenita (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
778377012 Paramyotonia congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229775013 Eulenburg's disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1229775013 Eulenburg's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1229776014 Eulenburg disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1229776014 Eulenburg disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424771001000116 Paramyotonia congenita Eulenburg de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
251331000172112 paramyotonie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
588931000172117 paramyotonia congenita fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
251331000172112 paramyotonie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
588931000172117 paramyotonia congenita fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3424771001000116 Paramyotonia congenita Eulenburg de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Paramyotonia congenita Is a Myopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Paramyotonia congenita Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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