230256009: Benign monomelic amyotrophy (disorder)

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

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Muscle atrophy\Benign monomelic amyotrophy

\Muscle finding (finding)\Disorder of muscle\...

\Degenerative disorder of muscle (disorder)\Muscle atrophy\Benign monomelic amyotrophy

\Disorder of skeletal muscle\Muscle atrophy\Benign monomelic amyotrophy

\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\...

\Degenerative disorder of musculoskeletal system (disorder)\Muscle atrophy\Benign monomelic amyotrophy

\Chronic disease of musculoskeletal system\Benign monomelic amyotrophy

\Disorder of skeletal muscle\Muscle atrophy\Benign monomelic amyotrophy

\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system (disorder)\Muscle atrophy\Benign monomelic amyotrophy
\Disease\Degenerative disorder\Degenerative disorder of muscle (disorder)\Muscle atrophy\Benign monomelic amyotrophy
\Disease\Disorder of body system\Disease of nervous system (disorder)\Chronic nervous system disorder (disorder)\Benign monomelic amyotrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Degenerative disorder of musculoskeletal system (disorder)\Muscle atrophy\Benign monomelic amyotrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Chronic disease of musculoskeletal system\Benign monomelic amyotrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Muscle atrophy\Benign monomelic amyotrophy
\Disease\Disorder of muscle\Degenerative disorder of muscle (disorder)\Muscle atrophy\Benign monomelic amyotrophy
\Disease\Disorder of muscle\Disorder of skeletal muscle\Muscle atrophy\Benign monomelic amyotrophy
\Disease\Chronic disease\Chronic nervous system disorder (disorder)\Benign monomelic amyotrophy
\Disease\Chronic disease\Chronic disease of musculoskeletal system\Benign monomelic amyotrophy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Muscle atrophy\Benign monomelic amyotrophy

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 monomelic amyotrophy	Is a	Disease of nervous system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign monomelic amyotrophy	Is a	Muscle atrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign monomelic amyotrophy	Finding site	Nervous system structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Benign monomelic amyotrophy	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Benign monomelic amyotrophy	Associated morphology	Atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Benign monomelic amyotrophy	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Benign monomelic amyotrophy	Associated morphology	Atrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Benign monomelic amyotrophy	Is a	Chronic nervous system disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign monomelic amyotrophy	Is a	Chronic disease of musculoskeletal system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign monomelic amyotrophy	Clinical course	Progressive	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Benign monomelic amyotrophy of lower limb	Is a	True	Benign monomelic amyotrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign monomelic amyotrophy of upper limb (disorder)	Is a	True	Benign monomelic amyotrophy	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
345073018	Benign monomelic amyotrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618038016	Benign monomelic amyotrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
345073018	Benign monomelic amyotrophy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
345073018	Benign monomelic amyotrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618038016	Benign monomelic amyotrophy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
618038016	Benign monomelic amyotrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3388451001000111	Amyotrophie, monomelische	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4957541000241117	amyotrophie monomélique bénigne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4957541000241117	amyotrophie monomélique bénigne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3388451001000111	Amyotrophie, monomelische	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module