240082006: myopathie met afwijking in histochemisch vezeltype (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\Myopathy with abnormality of histochemical fibre type

\Muscle finding\Disorder of muscle\...

\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type

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

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type

\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type
\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\Myopathy with abnormality of histochemical fibre type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type
\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\Myopathy with abnormality of histochemical fibre type
\Disease\Disorder of muscle\Congenital myopathy (disorder)\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type
\Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with abnormality of histochemical fibre type

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
Myopathy with abnormality of histochemical fibre type	Is a	Congenital myopathy	false	Inferred relationship	Some
Myopathy with abnormality of histochemical fibre type	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Myopathy with abnormality of histochemical fibre type	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Some
Myopathy with abnormality of histochemical fibre type	Finding site	Skeletal muscle system structure	false	Inferred relationship	Some
Myopathy with abnormality of histochemical fibre type	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	1
Myopathy with abnormality of histochemical fibre type	Occurrence	Congenital	false	Inferred relationship	Some
Myopathy with abnormality of histochemical fibre type	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Myopathy with abnormality of histochemical fibre type	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	1
Myopathy with abnormality of histochemical fibre type	Occurrence	Congenital	false	Inferred relationship	Some	2
Myopathy with abnormality of histochemical fibre type	Associated morphology	gebrekkige ontwikkeling (afwijkende morfologie)	false	Inferred relationship	Some	2
Myopathy with abnormality of histochemical fibre type	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Myopathy with abnormality of histochemical fibre type	Occurrence	Congenital	true	Inferred relationship	Some	1
Myopathy with abnormality of histochemical fibre type	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Myopathy with abnormality of histochemical fibre type	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Myopathy with type I hypotrophy	Is a	True	Myopathy with abnormality of histochemical fibre type	Inferred relationship	Some
Congenital myopathy with fibre type disproportion	Is a	True	Myopathy with abnormality of histochemical fibre type	Inferred relationship	Some
Congenital myopathy with uniform fiber type	Is a	True	Myopathy with abnormality of histochemical fibre type	Inferred relationship	Some
Congenital myopathy with reduced type 2 muscle fibers	Is a	True	Myopathy with abnormality of histochemical fibre type	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
359685013	Myopathy with abnormality of histochemical fibre type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
359686014	Myopathy with abnormality of histochemical fiber type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
629176019	Myopathy with abnormality of histochemical fiber type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
9189961000146110	myopathie met afwijking in histochemisch vezeltype (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9189971000146116	myopathie met afwijking in histochemisch vezeltype	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)