22131000146101: hereditaire 'inclusion body myositis' (aandoening)

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

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)

\Muscle finding\Disorder of muscle\...

\Hereditary myopathy (disorder)\Hereditary inclusion body myositis (disorder)

\Disorder of skeletal muscle\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)

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

\Hereditary disorder of musculoskeletal system\Hereditary inclusion body myositis (disorder)

\Inflammatory disorder of musculoskeletal system\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)

\Disorder of skeletal muscle\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary myopathy (disorder)\Hereditary inclusion body myositis (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of musculoskeletal system\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Inflammatory disorder of musculoskeletal system\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of muscle\Hereditary myopathy (disorder)\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of muscle\Disorder of skeletal muscle\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of musculoskeletal system\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Myositis\Inclusion body myositis\Hereditary inclusion body myositis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2020. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary inclusion body myositis (disorder)	Associated morphology	ontsteking (afwijkende morfologie)	false	Inferred relationship	Some	1
Hereditary inclusion body myositis (disorder)	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
Hereditary inclusion body myositis (disorder)	Is a	hereditaire inflammatoire aandoening	false	Inferred relationship	Some
Hereditary inclusion body myositis (disorder)	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Hereditary inclusion body myositis (disorder)	Is a	Inclusion body myositis	true	Inferred relationship	Some
Hereditary inclusion body myositis (disorder)	Is a	Hereditary myopathy (disorder)	true	Inferred relationship	Some
Hereditary inclusion body myositis (disorder)	Associated morphology	Inflammatory morphology (morphologic abnormality)	true	Inferred relationship	Some	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
161791000146110	Hereditary inclusion body myositis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
161801000146114	Hereditary inclusion body myositis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9072021000146111	erfelijke IBM	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
11937781000146110	hereditaire 'inclusion body myositis' (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
11937791000146112	hereditaire 'inclusion body myositis'	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)