703532002: 'cap'-myopathie (aandoening)

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

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Cap myopathy

\Muscle finding\Disorder of muscle\...

\Congenital myopathy (disorder)\Cap myopathy

\Hereditary myopathy (disorder)\Cap myopathy

\Disorder of skeletal muscle\Cap myopathy

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

\Hereditary disorder of musculoskeletal system\Cap myopathy

\Disorder of skeletal muscle\Cap myopathy

\Disease\Genetic disease\Hereditary disease\Hereditary myopathy (disorder)\Cap myopathy
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Cap myopathy
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Cap myopathy
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital myopathy (disorder)\Cap myopathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Cap myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Cap myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Cap myopathy
\Disease\Disorder of muscle\Congenital myopathy (disorder)\Cap myopathy
\Disease\Disorder of muscle\Hereditary myopathy (disorder)\Cap myopathy
\Disease\Disorder of muscle\Disorder of skeletal muscle\Cap myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Cap myopathy

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

Descriptions:

Id Description Lang Type Status Case? Module

3008914013 Cap myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3008979013 Cap disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009097013 Congenital myopathy with caps en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009579013 Cap myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6355731000146113 'cap'-myopathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6355761000146116 'cap'-myopathie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cap myopathy	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Cap myopathy	Is a	Congenital disease (disorder)	false	Inferred relationship	Some
Cap myopathy	Is a	Disorder of skeletal muscle	true	Inferred relationship	Some
Cap myopathy	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
Cap myopathy	Occurrence	Congenital	false	Inferred relationship	Some
Cap myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some
Cap myopathy	Occurrence	Congenital	true	Inferred relationship	Some	1
Cap myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Cap myopathy	Is a	Hereditary myopathy (disorder)	true	Inferred relationship	Some
Cap myopathy	Is a	Congenital myopathy (disorder)	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets