129622008: Nemaline myopathy, late onset type (disorder)

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

\General finding of soft tissue\Finding of power of skeletal muscle (finding)\Muscle weakness\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type
\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type

\Muscle finding (finding)\Finding of power of skeletal muscle (finding)\Muscle weakness\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type
\Muscle finding (finding)\Disorder of muscle\Disorder of skeletal muscle\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type

\Musculoskeletal finding (finding)\Finding of power of skeletal muscle (finding)\Muscle weakness\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type

\Disease\Genetic disease\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type
\Disease\Disorder of muscle\Disorder of skeletal muscle\Nemaline myopathy (disorder)\Nemaline myopathy, late onset type
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Nemaline myopathy (disorder)\Nemaline myopathy, late onset 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
Nemaline myopathy, late onset type	Is a	Nemaline myopathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Nemaline myopathy, late onset type	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Nemaline myopathy, late onset type	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Nemaline myopathy, late onset type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Nemaline myopathy, late onset type	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Nemaline myopathy, late onset type	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Nemaline myopathy, late onset type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Nemaline myopathy, late onset type	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Nemaline myopathy, late onset type	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Nemaline myopathy, late onset type	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Nemaline myopathy, late onset type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Nemaline myopathy, late onset type	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Nemaline myopathy, late onset type	Occurrence	Adulthood	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
208443016	Nemaline myopathy, late onset type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
733778012	Nemaline myopathy, late onset type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4695200018	Adult-onset nemaline myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
208443016	Nemaline myopathy, late onset type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
208443016	Nemaline myopathy, late onset type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
733778012	Nemaline myopathy, late onset type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
733778012	Nemaline myopathy, late onset type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4695200018	Adult-onset nemaline myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3424951001000114	Nemalin-Myopathie mit Beginn im Erwachsenenalter	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4790801000241119	myopathie à némaline à début tardif	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4790801000241119	myopathie à némaline à début tardif	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3424951001000114	Nemalin-Myopathie mit Beginn im Erwachsenenalter	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module