193222002: benigne congenitale myopathie (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\Benign congenital myopathy

\Muscle finding\Disorder of muscle\...

\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Benign congenital myopathy

\Hereditary myopathy (disorder)\Benign congenital myopathy

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy

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

\Hereditary disorder of musculoskeletal system\Benign congenital myopathy

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy

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

\Disease\Genetic disease\Hereditary disease\Hereditary myopathy (disorder)\Benign congenital myopathy
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Benign congenital myopathy
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Benign 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\Benign congenital myopathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign 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\Benign congenital myopathy
\Disease\Disorder of muscle\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Disorder of muscle\Hereditary myopathy (disorder)\Benign congenital myopathy
\Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Developmental disorder\Developmental hereditary disorder\Benign congenital myopathy
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign 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
Benign congenital myopathy	Is a	Muscular dystrophy	false	Inferred relationship	Some
Benign congenital myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Benign congenital myopathy	Associated morphology	Dystrophy	false	Inferred relationship	Some	1
Benign congenital myopathy	Is a	Congenital disease (disorder)	false	Inferred relationship	Some
Benign congenital myopathy	Occurrence	Congenital	false	Inferred relationship	Some
Benign congenital myopathy	Associated morphology	Dystrophy	false	Inferred relationship	Some	1
Benign congenital myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Benign congenital myopathy	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some
Benign congenital myopathy	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
Benign congenital myopathy	Occurrence	Congenital	false	Inferred relationship	Some	2
Benign congenital myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Benign congenital myopathy	Occurrence	Congenital	true	Inferred relationship	Some	1
Benign congenital myopathy	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Some
Benign congenital myopathy	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Benign congenital myopathy	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Benign congenital myopathy	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Benign congenital myopathy	Is a	Hereditary myopathy (disorder)	true	Inferred relationship	Some
Benign congenital myopathy	Is a	Congenital myopathy (disorder)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Benign Samaritan congenital myopathy (disorder)	Is a	True	Benign congenital myopathy	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
297605010	Benign congenital myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
577083019	Benign congenital myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6442621000146115	benigne congenitale myopathie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6442631000146118	benigne congenitale myopathie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6442641000146114	benigne aangeboren myopathie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)