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127954009: Skeletal muscle structure (body structure)

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

Descriptions:

Id Description Lang Type Status Case? Module
1241017 Skeletal muscle en Synonym Active Entire term case insensitive SNOMED CT core module
205212012 Striated muscle en Synonym Inactive Entire term case insensitive SNOMED CT core module
474270014 Skeletal muscle structure en Synonym Active Entire term case insensitive SNOMED CT core module
731896016 Skeletal muscle structure (body structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1764 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 Existential restriction modifier
Skeletal muscle structure Is a Skeletal and/or smooth muscle structure true Inferred relationship Existential restriction modifier
Skeletal muscle structure Part of Entire skeletal muscle system false Additional relationship Existential restriction modifier
Skeletal muscle structure Is a Structure of soft tissue true Inferred relationship Existential restriction modifier
Skeletal muscle structure Is a Skeletal muscle and/or tendon structure true Inferred relationship Existential restriction modifier
Skeletal muscle structure Is a Structure of striated muscle true Inferred relationship Existential restriction modifier
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 Existential restriction modifier 4
Injury of muscle(s) and tendon(s) of peroneal muscle group at lower leg level Finding site False Skeletal muscle structure Inferred relationship Existential restriction modifier 4
Injury of muscle and tendon at ankle and foot level Finding site False Skeletal muscle structure Inferred relationship Existential restriction modifier 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 Existential restriction modifier 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 Existential restriction modifier 4
Structure of extraocular muscle Is a True Skeletal muscle structure Inferred relationship Existential restriction modifier
Orbital myositis of left eye Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Orbital myositis of right eye Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Orbital myositis of bilateral eyes Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Rhabdomyolysis due to disease caused by severe acute respiratory syndrome coronavirus 2 Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Myopathy due to calcium deficiency Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Huntington's chorea Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 4
Juvenile onset Huntington's disease Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 6
Late onset Huntington's disease Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 6
Akinetic-rigid form of Huntington's disease Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 6
Hypotonic-hyporesponsive episode Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy type 1D large gene mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Crush syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Neostigmine test Procedure site - Indirect True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Ice pack test Procedure site - Indirect True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Crush syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Autosomal dominant Emery-Dreifuss muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Paresis of left vocal cord Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Paresis of right vocal cord Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Bilateral partial vocal cord paralysis Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Nontraumatic intramuscular hematoma Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Fibrous dysplasia of bone with intramuscular myxoma Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Neonatal neuromuscular disorder Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Hypomyopathic juvenile dermatomyositis Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Juvenile dermatomyositis overlap syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Juvenile polymyositis due to paraneoplastic syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Polymyositis overlap syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Dermatomyositis overlap syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Sporadic inclusion body myositis Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Paroxysmal rhabdomyolysis Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Microcephalus, brain defect, spasticity, hypernatremia syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 5
Myofascial pain syndrome of neck Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Autosomal recessive Emery-Dreifuss muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
X-linked Emery-Dreifuss muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Glycogen storage disease due to muscle beta-enolase deficiency Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Inflammation of skeletal muscle caused by Mycobacterium Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Adenylosuccinate synthetase-like 1-related distal myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Monocarboxylate transporter 8 deficiency Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Mitochondrial myopathy, lactic acidosis, deafness syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Combined oxidative phosphorylation defect type 30 Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Congenital generalized hypercontractile muscle stiffness syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Myotonic dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Blood vessel epicardial substance related limb girdle muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
LIM zinc finger domain containing 2-related limb girdle muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Glycogen storage disease due to lactate dehydrogenase deficiency Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Intellectual disability, epilepsy, extrapyramidal syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Maternally inherited mitochondrial myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Maternally inherited mitochondrial cardiomyopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Mitochondrial respiratory chain complex I structural subunit gene defect Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Mitochondrial respiratory chain complex I assembly gene defect Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Typical nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Childhood-onset nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Actin accumulation myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Amish nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Intermediate nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Severe congenital nemaline myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Lethal neonatal spasticity, epileptic encephalopathy syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Proximal myopathy with focal depletion of mitochondria Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Autosomal recessive central core disease Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal dominant central core disease Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Congenital fiber-type disproportion myopathy due to ZAK mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Congenital fiber-type disproportion myopathy due to selenoprotein N mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal recessive congenital fiber-type disproportion myopathy due to selenoprotein N mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal recessive congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Myasthenia gravis in remission Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Progressive scapulohumeroperoneal distal myopathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Autosomal dominant mitochondrial myopathy with exercise intolerance Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 4
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Intramuscular injection of human anti-D immunoglobulin Procedure site - Indirect True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Polyglucosan body myopathy type 2 Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 3
Megaconial congenital muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 1
Megaconial congenital muscular dystrophy Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2
Hereditary continuous muscle fiber activity Finding site True Skeletal muscle structure Inferred relationship Existential restriction modifier 2

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