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43152001: Central core disease (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\Central core disease

\Muscle finding\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease

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

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease

\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease
\Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Central core disease	Is a	Congenital myopathy	false	Inferred relationship	Some
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Central core disease	Associated morphology	Central cores	true	Inferred relationship	Some	1
Central core disease	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Some
Central core disease	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some
Central core disease	Occurrence	Congenital	false	Inferred relationship	Some
Central core disease	Associated morphology	kongenital anomali	false	Inferred relationship	Some	2
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Central core disease	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Central core disease	Occurrence	Congenital	false	Inferred relationship	Some	3
Central core disease	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	3
Central core disease	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	3
Central core disease	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Central core disease	Occurrence	Congenital	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
71981018	Central core disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
780131019	Central core disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2966549015	Central core myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1983401000052110	central core disease	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)