55133004: multicoremyopathie (aandoening)

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

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy

\Muscle finding\Disorder of muscle\...

\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy

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

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy

\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy
\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\Multi-core congenital myopathy
\Disease\Disorder of muscle\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy
\Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Multi-core congenital myopathy

Status: current, Not 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
Multi-core congenital myopathy	Is a	Congenital myopathy	false	Inferred relationship	Some
Multi-core congenital myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Multi-core congenital myopathy	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some
Multi-core congenital myopathy	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Some
Multi-core congenital myopathy	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	1
Multi-core congenital myopathy	Occurrence	Congenital	false	Inferred relationship	Some
Multi-core congenital myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Multi-core congenital myopathy	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	1
Multi-core congenital myopathy	Occurrence	Congenital	false	Inferred relationship	Some	2
Multi-core congenital myopathy	Associated morphology	gebrekkige ontwikkeling (afwijkende morfologie)	false	Inferred relationship	Some	2
Multi-core congenital myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Multi-core congenital myopathy	Occurrence	Congenital	true	Inferred relationship	Some	1
Multi-core congenital myopathy	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Multi-core congenital myopathy	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Antenatal multi-minicore disease with arthrogryposis multiplex congenita	Is a	True	Multi-core congenital myopathy	Inferred relationship	Some
Congenital multi-minicore disease with external ophthalmoplegia (disorder)	Is a	True	Multi-core congenital myopathy	Inferred relationship	Some

Reference Sets

Dutch rare neuromuscular disorders simple reference set (foundation metadata concept)

Dutch pathology simple reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
91653017	Multi-core congenital myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
91654011	Multi-core disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
793441013	Multi-core congenital myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1231419016	Minicore disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1231420010	Multicore disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3033415015	Multiminicore disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3033531013	Multi-minicore disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
119991000146113	multicoremyopathie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
936081000146111	multicoremyopathie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)