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

\Muscle finding\Disorder of muscle\...

\Degenerative disorder of muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy

\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy

\Musculoskeletal finding\Disorder of musculoskeletal system\...

\Degenerative disorder of musculoskeletal system\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy

\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy

\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy
\Disease\Degenerative disorder\Degenerative disorder of muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy
\Disease\Degenerative disorder\Amyloidosis\Amyloid myopathy\Primary familial amyloid myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Degenerative disorder of musculoskeletal system\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy
\Disease\Disorder of muscle\Degenerative disorder of muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy
\Disease\Disorder of muscle\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Deposition in skeletal muscle\Amyloid myopathy\Primary familial amyloid myopathy

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

7656231000172112 myopathie amyloïde primaire familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

7656241000172117 myopathie amyloïde primitive familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

5528871000172117 primaire familiale amyloïde myopathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary familial amyloid myopathy	Is a	Amyloid myopathy	true	Inferred relationship	Some
Primary familial amyloid myopathy	Associated morphology	Amyloid deposition	false	Inferred relationship	Some	1
Primary familial amyloid myopathy	Finding site	Skeletal muscle structure (body structure)	false	Inferred relationship	Some	1
Primary familial amyloid myopathy	Associated morphology	Amyloid deposition	true	Inferred relationship	Some	1
Primary familial amyloid myopathy	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