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127954009: Skeletal muscle structure (body structure)

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
1241017 Skeletal muscle en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
205212012 Striated muscle en Synonym (core metadata concept) Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
474270014 Skeletal muscle structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
731896016 Skeletal muscle structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
275041000077112 structure de muscle squelettique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1768 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Skeletal muscle structure Is a Skeletal muscle system structure false Inferred relationship Some
Skeletal muscle structure Is a Skeletal and/or smooth muscle structure (body structure) true Inferred relationship Some
Skeletal muscle structure partie de Entire skeletal muscle system (body structure) false Additional relationship Some
Skeletal muscle structure Is a Structure of soft tissue (body structure) true Inferred relationship Some
Skeletal muscle structure Is a Skeletal muscle and/or tendon structure true Inferred relationship Some
Skeletal muscle structure Is a Structure of striated muscle true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Injury of muscle(s) and tendon(s) of anterior muscle group at lower leg level Finding site False Skeletal muscle structure Inferred relationship Some 4
Injury of muscle(s) and tendon(s) of peroneal muscle group at lower leg level Finding site False Skeletal muscle structure Inferred relationship Some 4
Injury of muscle and tendon at ankle and foot level Finding site False Skeletal muscle structure Inferred relationship Some 4
Injury of muscle and tendon of long flexor muscle of toe at ankle and foot level Finding site False Skeletal muscle structure Inferred relationship Some 4
Injury of muscle and tendon of long extensor muscle of toe at ankle and foot level Finding site False Skeletal muscle structure Inferred relationship Some 4
Structure of extraocular muscle Is a True Skeletal muscle structure Inferred relationship Some
Orbital myositis of left eye Finding site True Skeletal muscle structure Inferred relationship Some 2
Orbital myositis of right eye Finding site True Skeletal muscle structure Inferred relationship Some 2
Bilateral orbital myositis of eyes Finding site True Skeletal muscle structure Inferred relationship Some 3
Rhabdomyolysis due to disease caused by severe acute respiratory syndrome coronavirus 2 (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 2
Myopathy due to calcium deficiency (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 2
Huntington's chorea Finding site True Skeletal muscle structure Inferred relationship Some 4
Juvenile onset Huntington's disease Finding site True Skeletal muscle structure Inferred relationship Some 6
Late onset Huntington's disease Finding site True Skeletal muscle structure Inferred relationship Some 6
Akinetic-rigid form of Huntington's disease Finding site True Skeletal muscle structure Inferred relationship Some 6
Hypotonic-hyporesponsive episode (finding) Finding site True Skeletal muscle structure Inferred relationship Some 3
Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Congenital muscular dystrophy type 1D large gene mutation (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Crush syndrome Finding site True Skeletal muscle structure Inferred relationship Some 1
Neostigmine test Procedure site - Indirect (attribute) True Skeletal muscle structure Inferred relationship Some 1
Ice pack test Procedure site - Indirect (attribute) True Skeletal muscle structure Inferred relationship Some 1
Crush syndrome Finding site True Skeletal muscle structure Inferred relationship Some 3
Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Paresis of left vocal cord (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
Paresis of right vocal cord (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
Bilateral partial vocal cord paralysis Finding site True Skeletal muscle structure Inferred relationship Some 1
Nontraumatic intramuscular haematoma Finding site True Skeletal muscle structure Inferred relationship Some 1
Fibrous dysplasia of bone with intramuscular myxoma Finding site True Skeletal muscle structure Inferred relationship Some 1
Neonatal neuromuscular disorder Finding site True Skeletal muscle structure Inferred relationship Some 1
Hypomyopathic juvenile dermatomyositis Finding site True Skeletal muscle structure Inferred relationship Some 1
Juvenile dermatomyositis overlap syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
Juvenile polymyositis due to paraneoplastic syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Polymyositis overlap syndrome Finding site True Skeletal muscle structure Inferred relationship Some 2
Dermatomyositis overlap syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
Sporadic inclusion body myositis (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Paroxysmal rhabdomyolysis (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 5
Myofascial pain syndrome of neck Finding site True Skeletal muscle structure Inferred relationship Some 3
Autosomal recessive Emery-Dreifuss muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Some 1
X-linked Emery-Dreifuss muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Some 1
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency Finding site True Skeletal muscle structure Inferred relationship Some 2
Glycogen storage disease due to muscle beta-enolase deficiency Finding site True Skeletal muscle structure Inferred relationship Some 1
Mycobacterial myositis Finding site True Skeletal muscle structure Inferred relationship Some 1
Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome Finding site True Skeletal muscle structure Inferred relationship Some 2
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Adenylosuccinate synthetase-like 1-related distal myopathy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
POGLUT1-related limb girdle muscular dystrophy R21 Finding site True Skeletal muscle structure Inferred relationship Some 1
Allan-Herndon-Dudley syndrome Finding site True Skeletal muscle structure Inferred relationship Some 2
Mitochondrial myopathy, lactic acidosis, deafness syndrome Finding site True Skeletal muscle structure Inferred relationship Some 3
Combined oxidative phosphorylation defect type 30 Finding site True Skeletal muscle structure Inferred relationship Some 3
Congenital generalized hypercontractile muscle stiffness syndrome Finding site True Skeletal muscle structure Inferred relationship Some 2
Myotonic dystrophy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome Finding site True Skeletal muscle structure Inferred relationship Some 1
Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
LIMS2-related limb girdle muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Some 1
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
Glycogen storage disease due to lactate dehydrogenase deficiency Finding site True Skeletal muscle structure Inferred relationship Some 1
Intellectual disability, epilepsy, extrapyramidal syndrome Finding site True Skeletal muscle structure Inferred relationship Some 1
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome Finding site True Skeletal muscle structure Inferred relationship Some 1
Maternally inherited mitochondrial myopathy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Maternally inherited mitochondrial cardiomyopathy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
Mitochondrial respiratory chain complex I structural subunit gene defect Finding site True Skeletal muscle structure Inferred relationship Some 2
Mitochondrial respiratory chain complex I assembly gene defect Finding site True Skeletal muscle structure Inferred relationship Some 2
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 2
Typical nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Some 1
Childhood-onset nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Some 1
Actin accumulation myopathy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Amish nemaline myopathy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Intermediate nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Some 1
Severe congenital nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Some 1
Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Proximal myopathy with focal depletion of mitochondria Finding site True Skeletal muscle structure Inferred relationship Some 2
Autosomal recessive central core disease Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal dominant central core disease (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Congenital fiber-type disproportion myopathy due to ZAK mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Congenital fiber-type disproportion myopathy due to SELENON mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal dominant congenital fibre-type disproportion myopathy due to SELENON mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal recessive congenital fiber-type disproportion myopathy due to selenoprotein N mutation (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Congenital fibre-type disproportion myopathy due to ACTA1 mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal recessive congenital fibre-type disproportion myopathy due to ACTA1 mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal dominant congenital fibre-type disproportion myopathy due to ACTA1 mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Congenital fiber-type disproportion myopathy due to TPM3 mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Autosomal dominant congenital fiber-type disproportion myopathy due to TPM3 mutation Finding site True Skeletal muscle structure Inferred relationship Some 1
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Finding site True Skeletal muscle structure Inferred relationship Some 2
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies Finding site True Skeletal muscle structure Inferred relationship Some 2
Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Myasthenia gravis in remission Finding site True Skeletal muscle structure Inferred relationship Some 1
Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome Finding site True Skeletal muscle structure Inferred relationship Some 3
Progressive scapulohumeroperoneal distal myopathy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 1
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 3
Autosomal dominant mitochondrial myopathy with exercise intolerance Finding site True Skeletal muscle structure Inferred relationship Some 2
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 4
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) Finding site True Skeletal muscle structure Inferred relationship Some 2
Intramuscular injection of human anti-D immunoglobulin Procedure site - Indirect (attribute) True Skeletal muscle structure Inferred relationship Some 1
Polyglucosan body myopathy type 2 Finding site True Skeletal muscle structure Inferred relationship Some 3
Megaconial congenital muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Some 1
Megaconial congenital muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Some 2
Hereditary continuous muscle fiber activity Finding site True Skeletal muscle structure Inferred relationship Some 2

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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