20305008: Congenital myotonia, autosomal recessive form (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Myotonic disorder\Myotonia congenita\Congenital myotonia, autosomal recessive form
• \Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Myotonic disorder\Myotonia congenita\Congenital myotonia, autosomal recessive form
• \Musculoskeletal finding\Disorder of musculoskeletal system\...
• \Hereditary disorder of musculoskeletal system\Congenital myotonia, autosomal recessive form
• \Disorder of skeletal muscle\Myotonic disorder\Myotonia congenita\Congenital myotonia, autosomal recessive form
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Congenital myotonia, autosomal recessive form
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Congenital myotonia, autosomal recessive form
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Congenital myotonia, autosomal recessive form
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Congenital myotonia, autosomal recessive form
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Myotonic disorder\Myotonia congenita\Congenital myotonia, autosomal recessive form
• \Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Myotonic disorder\Myotonia congenita\Congenital myotonia, autosomal recessive form
• \Disease\Congenital disease\Myotonia congenita\Congenital myotonia, autosomal recessive form
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Myotonic disorder\Myotonia congenita\Congenital myotonia, autosomal recessive form

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
34147015	Congenital myotonia, autosomal recessive form	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
749363012	Congenital myotonia, autosomal recessive form (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1222419014	Becker myotonia congenita	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
1222420015	Myotonia congenita - autosomal recessive form	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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