763895001: Myosclerosis (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Myosclerosis
• \Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Myosclerosis
• \Musculoskeletal finding\Disorder of musculoskeletal system\...
• \Hereditary disorder of musculoskeletal system\Myosclerosis
• \Disorder of skeletal muscle\Myosclerosis
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Myosclerosis
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Myosclerosis
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Myosclerosis
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Myosclerosis
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Myosclerosis
• \Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Myosclerosis
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Myosclerosis
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Myosclerosis
• \Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Myosclerosis
• \Disease\Congenital disease\Myosclerosis
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Myosclerosis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3645182013	Myosclerosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3645183015	Myosclerosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3670041015	Congenital myosclerosis Lowenthal type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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