267607008: Familial periodic paralysis (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation générale à propos des tissus mous\Disorder of soft tissue\affection d'un muscle squelettique\myopathie d'origine métabolique (trouble)\paralysie périodique familiale

\constatation à propos d'un muscle\affection musculaire\affection d'un muscle squelettique\myopathie d'origine métabolique (trouble)\paralysie périodique familiale

\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\affection d'un muscle squelettique\myopathie d'origine métabolique (trouble)\paralysie périodique familiale

\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\affection d'un muscle squelettique\myopathie d'origine métabolique (trouble)\paralysie périodique familiale
\Disease\affection musculaire\affection d'un muscle squelettique\myopathie d'origine métabolique (trouble)\paralysie périodique familiale
\Disease\Disorder of soft tissue\affection d'un muscle squelettique\myopathie d'origine métabolique (trouble)\paralysie périodique familiale

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

120961000172112 paralysie périodique familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

399422014 Familial periodic paralysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

399423016 Myoplegic dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

399424010 Familial recurrent paralysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

399425011 Familial myoplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

399427015 Cavarre disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

399428013 Periodic myotonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

564991000241116 paralysie périodique familiale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

660244012 Familial periodic paralysis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
paralysie périodique familiale	localisation d'une constatation (attribut)	structure de muscle squelettique	true	Inferred relationship	Some	1
paralysie périodique familiale	est un(e) (attribut)	myopathie d'origine métabolique (trouble)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial hyperkalemic periodic paralysis	est un(e) (attribut)	True	paralysie périodique familiale	Inferred relationship	Some
Westphal disease	est un(e) (attribut)	False	paralysie périodique familiale	Inferred relationship	Some
paralysie périodique thyrotoxique (trouble)	est un(e) (attribut)	True	paralysie périodique familiale	Inferred relationship	Some
Familial normokalaemic periodic paralysis	est un(e) (attribut)	True	paralysie périodique familiale	Inferred relationship	Some
Familial hypokalemic periodic paralysis	est un(e) (attribut)	True	paralysie périodique familiale	Inferred relationship	Some
Hypokalemic periodic paralysis	est un(e) (attribut)	False	paralysie périodique familiale	Inferred relationship	Some
Familial hyperkalemic periodic paralysis	est un(e) (attribut)	False	paralysie périodique familiale	Inferred relationship	Some

This concept is not in any reference sets