237873000: Primary familial amyloid myopathy (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy (disorder)
• \Muscle finding (finding)\Disorder of muscle\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy (disorder)
• \Disease\Disorder of muscle\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy (disorder)
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy (disorder)
• \Disease\Amyloidosis\Amyloid myopathy\Primary familial amyloid myopathy (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
356483013	Primary familial amyloid myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626664017	Primary familial amyloid myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
356483013	Primary familial amyloid myopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
356483013	Primary familial amyloid myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626664017	Primary familial amyloid myopathy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
626664017	Primary familial amyloid myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5020801000241115	myopathie amyloïde primaire familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5020801000241115	myopathie amyloïde primaire familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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