1222644009: Autosomal dominant mitochondrial myopathy with exercise intolerance (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Muscle finding\Disorder of muscle\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Musculoskeletal finding\Disorder of musculoskeletal system\...
• \Hereditary disorder of musculoskeletal system\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Chronic disease of musculoskeletal system\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Disorder of muscle\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Metabolic disease\Mitochondrial cytopathy (disorder)\Mitochondrial myopathy\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Metabolic disease\Chronic metabolic disorder\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Chronic disease\Chronic metabolic disorder\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Chronic disease\Chronic disease of musculoskeletal system\Autosomal dominant mitochondrial myopathy with exercise intolerance
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Autosomal dominant mitochondrial myopathy with exercise intolerance

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5048276010	Autosomal dominant mitochondrial myopathy with exercise intolerance	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5048277018	Autosomal dominant mitochondrial myopathy with exercise intolerance (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5399976013	A rare mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies characterized by onset of slowly progressive proximal lower limb weakness and exercise intolerance in the first decade of life, followed by weakness of neck flexor, shoulder, and distal leg muscles. Facial muscles become involved still later in the disease course. Additional manifestations are restrictive pulmonary function and short stature. Laboratory studies reveal lactic acidemia and increased serum creatine kinase.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399977016	A rare mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies characterised by onset of slowly progressive proximal lower limb weakness and exercise intolerance in the first decade of life, followed by weakness of neck flexor, shoulder, and distal leg muscles. Facial muscles become involved still later in the disease course. Additional manifestations are restrictive pulmonary function and short stature. Laboratory studies reveal lactic acidaemia and increased serum creatine kinase.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start