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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
251331000172112 paramyotonie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
11544361000172110 paramyotonia congenita fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
120511000172119 paramyotonia congenita 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
Paramyotonia congenita (disorder) Is a Myotonic disorder true Inferred relationship Some
Paramyotonia congenita (disorder) Is a Myopathy false Inferred relationship Some
Paramyotonia congenita (disorder) Finding site Skeletal 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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