43226001: Sarcotubular myopathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Sarcotubular myopathy

\Muscle finding\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Sarcotubular myopathy

\Musculoskeletal finding\Disorder of musculoskeletal system (disorder)\...

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Sarcotubular myopathy

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Sarcotubular myopathy

\Disease\Fetal and/or neonatal disorder\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Sarcotubular myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Sarcotubular myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Sarcotubular myopathy
\Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Sarcotubular myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Sarcotubular myopathy
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Sarcotubular 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

72118015 Sarcotubular myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

780213011 Sarcotubular myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4530881000241119 myopathie sarcotubulaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3436461001000114 TRIM32-assoziierte Gliedergürtelmuskeldystrophie R8 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sarcotubular myopathy	Is a	Congenital myopathy	false	Inferred relationship	Some
Sarcotubular myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Sarcotubular myopathy	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Some
Sarcotubular myopathy	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some
Sarcotubular myopathy	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	1
Sarcotubular myopathy	Occurrence	Congenital	false	Inferred relationship	Some
Sarcotubular myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Sarcotubular myopathy	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	1
Sarcotubular myopathy	Occurrence	Congenital	false	Inferred relationship	Some	2
Sarcotubular myopathy	Associated morphology	anomalie du développement	false	Inferred relationship	Some	2
Sarcotubular myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Sarcotubular myopathy	Occurrence	Congenital	true	Inferred relationship	Some	1
Sarcotubular myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Sarcotubular myopathy	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Sarcotubular myopathy	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1

Inbound Relationships

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Active

Source

Characteristic

Refinability

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Reference Sets

Description inactivation indicator reference set