764945007: Congenital myopathy with internal nuclei and atypical cores (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Musculoskeletal finding\Disorder of musculoskeletal system\...
• \Hereditary disorder of musculoskeletal system\Congenital myopathy with internal nuclei and atypical cores
• \Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Developmental disorder\Developmental hereditary disorder\Congenital myopathy with internal nuclei and atypical cores
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Congenital myopathy with internal nuclei and atypical cores

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
3655707019	Centronuclear myopathy type 4	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3655708012	Congenital myopathy with internal nuclei and atypical cores (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3655709016	Congenital myopathy with internal nuclei and atypical cores	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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