699267007: Myosin storage myopathy (disorder)

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

\General finding of soft tissue\Finding of power of skeletal muscle\Muscle weakness\Myosin storage myopathy (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Myosin storage myopathy (disorder)

\Muscle finding\Finding of power of skeletal muscle\Muscle weakness\Myosin storage myopathy (disorder)
\Muscle finding\Disorder of muscle\Disorder of skeletal muscle\Myosin storage myopathy (disorder)

\Musculoskeletal finding\Finding of power of skeletal muscle\Muscle weakness\Myosin storage myopathy (disorder)
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Myosin storage myopathy (disorder)
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal muscle\Myosin storage myopathy (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Myosin storage myopathy (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Myosin storage myopathy (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Myosin storage myopathy (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Myosin storage myopathy (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Myosin storage myopathy (disorder)
\Disease\Disorder of muscle\Disorder of skeletal muscle\Myosin storage myopathy (disorder)
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Myosin storage myopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2983424016 Myosin storage myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2983446012 Myosin storage myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5170018018 Hyaline body myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

7686431000172115 myopathie à corps hyalins autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

7686441000172110 myopathie causée par une accumulation de myosine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

5566641000172118 autosomal dominant hyaline body myopathy nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

5566651000172116 myosine-opslag myopathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Myosin storage myopathy (disorder)	Is a	Disorder of skeletal muscle	true	Inferred relationship	Some
Myosin storage myopathy (disorder)	Finding site	Skeletal muscle structure (body structure)	true	Inferred relationship	Some	1
Myosin storage myopathy (disorder)	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Myosin storage myopathy (disorder)	Is a	Muscle weakness	true	Inferred relationship	Some
Myosin storage myopathy (disorder)	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets