60738003: Secondary myopathy (disorder)

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

\Muscle finding\Disorder of muscle\Secondary myopathy

\Disease\Disorder of muscle\Secondary myopathy

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

Descriptions:

Id Description Lang Type Status Case? Module

100922013 Secondary myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

799723014 Secondary myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6924251000241117 myopathie secondaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Secondary myopathy	Is a	Myopathy	false	Inferred relationship	Some
Secondary myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Secondary myopathy	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some
Secondary myopathy	Is a	Disorder of muscle	true	Inferred relationship	Some
Secondary myopathy	Finding site	Skeletal and/or smooth muscle structure (body structure)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sarcoid myopathy	Is a	True	Secondary myopathy	Inferred relationship	Some
Human immunodeficiency virus myopathy	Is a	True	Secondary myopathy	Inferred relationship	Some
Steroid-induced myopathy	Is a	False	Secondary myopathy	Inferred relationship	Some
Carcinomatous myopathic syndrome (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
myopathie inflammatoire symptomatique associée à un autre trouble	Is a	False	Secondary myopathy	Inferred relationship	Some
Symptomatic inflammatory myopathy in disease NOS	Is a	False	Secondary myopathy	Inferred relationship	Some
Autoimmune myopathy (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Drug-induced myopathy	Is a	False	Secondary myopathy	Inferred relationship	Some
Toxic myopathy	Is a	True	Secondary myopathy	Inferred relationship	Some
Thyroid eye disease	Is a	True	Secondary myopathy	Inferred relationship	Some
Myopathy due to Sjögren's disease (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Protein deficiency myopathy	Is a	True	Secondary myopathy	Inferred relationship	Some
Paraneoplastic myositis	Is a	True	Secondary myopathy	Inferred relationship	Some
Contracture of gastrocnemius muscle due to traumatic injury (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Myopathy due to scleroderma	Is a	True	Secondary myopathy	Inferred relationship	Some
Rhabdomyolysis due to disease caused by severe acute respiratory syndrome coronavirus 2 (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Myopathy due to calcium deficiency (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Ocular torticolis	Is a	True	Secondary myopathy	Inferred relationship	Some
Weakness of face muscles as sequela of stroke	Is a	True	Secondary myopathy	Inferred relationship	Some
Weakness of extremities as sequela of stroke	Is a	True	Secondary myopathy	Inferred relationship	Some
Spasticity as sequela of stroke (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome is a rare mitochondrial disease with marked clinical variability typically characterized by encephalomyopathy, kidney disease (nephrotic syndrome), optic atrophy, early-onset deafness, pancytopenia, obesity, and cardiac disease (valvulopathy). Additionally, macrocephaly, intellectual disability, hyperlactatemia, elevated lactate/pyruvate ratio, insulin-dependent diabetes, livedo reticularis, liver dysfunction and seizures have also been associated.	Is a	True	Secondary myopathy	Inferred relationship	Some
A mitochondrial oxidative phosphorylation disorder characterized by hypertrophic and dilated cardiomyopathy, failure to thrive, myopathy with generalized hypotonia and increased creatine kinase, developmental delay and/or regression with cerebral atrophy on brain MRI, renal manifestations including chronic renal failure, renal tubular acidosis and lactic acidosis. Additional clinical features include seizures and respiratory failure.	Is a	True	Secondary myopathy	Inferred relationship	Some
Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy (CCM) is a mitochondrial disease characterized by cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise.	Is a	True	Secondary myopathy	Inferred relationship	Some
Cardiomyopathy-hypotonia-lactic acidosis syndrome is characterized by hypertrophic cardiomyopathy, muscular hypotonia and the presence of lactic acidosis at birth. It has been described in two sisters (both of whom died within the first year of life) from a nonconsanguineous Turkish family. The syndrome is caused by a homozygous point mutation in the exon 3A of the SLC25A3 gene encoding a mitochondrial membrane transporter.	Is a	True	Secondary myopathy	Inferred relationship	Some
Myopathy co-occurrent and due to hypercalcemia (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Glycogen storage disease due to muscle and heart glycogen synthase deficiency is characterized by muscle and heart glycogen deficiency. It has been described in three siblings (two brothers and their younger sister). The older brother died at 10.5 years of age as a result of sudden cardiac arrest and the younger brother presented with hypertrophic cardiomyopathy, abnormal heart rate and blood pressure during exercise, and muscle fatigability. The sister showed no symptoms but a lack of glycogen was identified through muscle biopsy. The syndrome is caused by homozygous missense mutations in the gene encoding muscle glycogen synthase.	Is a	True	Secondary myopathy	Inferred relationship	Some
A rare mitochondrial disease characterized by adult onset of the triad of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis. Additional signs and symptoms are highly variable and include myopathy, seizures, and hearing loss, among others. Brain imaging may show cerebellar white matter abnormalities and/or bilateral thalamic lesions.	Is a	True	Secondary myopathy	Inferred relationship	Some
Necrosis of muscle of buttock co-occurrent and due to chronic ulcer of buttock (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Weakness of right facial muscle due to and following cerebrovascular disease (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Weakness of left facial muscle due to and following cerebrovascular disease (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Spasmodic torticollis due to infection	Is a	True	Secondary myopathy	Inferred relationship	Some
Necrosis of ankle muscle co-occurrent and due to chronic ulcer of ankle (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Myopathy due to Cushing's syndrome	Is a	True	Secondary myopathy	Inferred relationship	Some
Necrosis of lower leg muscle co-occurrent and due to chronic ulcer of lower leg	Is a	True	Secondary myopathy	Inferred relationship	Some
A rare glycolysis disorder characterized clinically by exercise intolerance and myalgia due to severe enolase deficiency in muscle.	Is a	True	Secondary myopathy	Inferred relationship	Some
Maternally inherited mitochondrial cardiomyopathy and myopathy	Is a	True	Secondary myopathy	Inferred relationship	Some
A rare mitochondrial disease characterized by neonatal onset of severe cardiac and/or neurologic signs and symptoms mostly associated with a fatal outcome in the neonatal period or in infancy, although a milder phenotype with later onset and slowly progressive neurologic deterioration has also been reported. Clinical manifestations are variable and include respiratory insufficiency, hypotonia, cardiomyopathy, and seizures. Serum lactate is elevated in most cases. Brain imaging may show cerebellar atrophy or hypoplasia.	Is a	True	Secondary myopathy	Inferred relationship	Some
Glycogen storage disease due to lactate dehydrogenase deficiency	Is a	True	Secondary myopathy	Inferred relationship	Some
Maternally inherited mitochondrial myopathy (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Maternally inherited mitochondrial cardiomyopathy (disorder)	Is a	False	Secondary myopathy	Inferred relationship	Some
Myopathy of extraocular muscle due to disorder of blood vessel (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Incomplete closure of velopharyngeal apparatus due to cleft palate	Is a	True	Secondary myopathy	Inferred relationship	Some
Weakness of facial muscle due to and following non-traumatic intracranial subarachnoid hemorrhage (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Volkmann contracture	Is a	True	Secondary myopathy	Inferred relationship	Some
Foreign body granuloma of muscle	Is a	True	Secondary myopathy	Inferred relationship	Some
Myopathy due to chronic alcoholism (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Myopathy due to magnesium deficiency (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Allergic bronchospasm caused by dietary substance (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Bronchospasm caused by drug	Is a	True	Secondary myopathy	Inferred relationship	Some
Anaerobic myonecrosis	Is a	True	Secondary myopathy	Inferred relationship	Some
Disorder of muscle due to paraneoplastic syndrome (disorder)	Is a	True	Secondary myopathy	Inferred relationship	Some
Calcification of muscle due to adult dermatomyositis	Is a	True	Secondary myopathy	Inferred relationship	Some
Calcification of muscle due to juvenile dermatomyositis	Is a	True	Secondary myopathy	Inferred relationship	Some
Traumatic myositis ossificans	Is a	True	Secondary myopathy	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
100922013	Secondary myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
799723014	Secondary myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6924251000241117	myopathie secondaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module