74035001: Denervation atrophy of muscle (disorder)

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

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Muscle atrophy\Denervation atrophy of muscle

\Muscle finding\Disorder of muscle\...

\Degenerative disorder of muscle\Muscle atrophy\Denervation atrophy of muscle

\Disorder of skeletal muscle\Muscle atrophy\Denervation atrophy of muscle

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

\Degenerative disorder of musculoskeletal system\Muscle atrophy\Denervation atrophy of muscle

\Disorder of skeletal muscle\Muscle atrophy\Denervation atrophy of muscle

\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system\Muscle atrophy\Denervation atrophy of muscle
\Disease\Degenerative disorder\Degenerative disorder of muscle\Muscle atrophy\Denervation atrophy of muscle
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Degenerative disorder of musculoskeletal system\Muscle atrophy\Denervation atrophy of muscle
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Muscle atrophy\Denervation atrophy of muscle
\Disease\Disorder of muscle\Degenerative disorder of muscle\Muscle atrophy\Denervation atrophy of muscle
\Disease\Disorder of muscle\Disorder of skeletal muscle\Muscle atrophy\Denervation atrophy of muscle
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Muscle atrophy\Denervation atrophy of muscle

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

Descriptions:

Id Description Lang Type Status Case? Module

122935017 Denervation atrophy of muscle en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

122936016 Group atrophy of muscle fibers en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

122937013 Neurogenic muscular atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

502589010 Group atrophy of muscle fibres en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

814490012 Denervation atrophy of muscle (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4632451000241119 amyotrophie de dénervation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Denervation atrophy of muscle	Is a	Muscle atrophy	true	Inferred relationship	Some
Denervation atrophy of muscle	Associated morphology	Muscle fiber atrophy	false	Inferred relationship	Some	2
Denervation atrophy of muscle	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Denervation atrophy of muscle	Associated morphology	Atrophy	false	Inferred relationship	Some	1
Denervation atrophy of muscle	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Denervation atrophy of muscle	Associated morphology	Atrophy	false	Inferred relationship	Some	1
Denervation atrophy of muscle	Due to	Denervation	true	Inferred relationship	Some	2
Denervation atrophy of muscle	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some
Denervation atrophy of muscle	Associated morphology	Muscle fiber atrophy	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Stringhalt	Is a	False	Denervation atrophy of muscle	Inferred relationship	Some
Denervation atrophy of tongue (disorder)	Is a	True	Denervation atrophy of muscle	Inferred relationship	Some
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy.	Due to	True	Denervation atrophy of muscle	Inferred relationship	Some	3
A rare, multisystem disorder, characterized by neurogenic arthrogryposis multiplex congenita, renal tubular dysfunction and neonatal cholestasis with low serum gamma-glutamyl transferase activity.	Due to	True	Denervation atrophy of muscle	Inferred relationship	Some	3

This concept is not in any reference sets