Skeletal muscle structure
Skeletal muscle
Striated muscle
Skeletal muscle structure (body structure)
127954009
http://purl.bioontology.org/ontology/SNOMEDCT/127954009
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Xa1Pu
Decompression of thoracic outlet by myotomy of scalenus anticus muscle
Stretching of muscle
Local muscle subcutaneous V-Y flap
Local muscle transposition flap
Debridement of muscle
Replacement of skeletal muscle stimulator
Biopsy of skeletal muscle
Repair of muscle by graft or implant of fascia
Advancement of muscle
Release of contracture of muscle
Tensing of orbicularis oculi muscle
Repair of muscle by graft or implant of tendon
Bone division and muscle transfer
Lengthening of tendon or muscle
Excision of myositis ossificans
Biceps tunnel cineplasty
Plastic operation on muscle
Distal recession of gastrocnemius
Adjustment to length of tendon or muscle
Flexorplasty of elbow
Wide excision of muscle tissue
Shortening of muscle
Local muscle rotation flap
Decompression of muscle
Curettage of muscle
Grafting of muscle
Change of length of muscle
Muscle-testing electrodiagnosis with chronaximetry
Debridement of skin, subcutaneous tissue, muscle and bone
Harvest of muscle flap
Release of paralytic tether
Myectomy for graft
Distant muscle subcutaneous pedicle flap
Physiatric stretching of muscle
Muscle transfer for claw toe repair
Lengthening of muscle
Muscle-testing by bicycle dynamometer
Harvesting of muscle
Destruction of lesion of muscle
Distant muscle microvascular free flap
Debridement of skin, subcutaneous tissue and muscle
Local muscle subcutaneous pedicle island flap
Release of Volkmann's contracture by muscle transplantation
Release of muscle origin
Plication of recti
Recession of muscle
Myotenontoplasty of hand
Mammoplasty with muscle flap
Biopsy of lesion of muscle
Transfer of hand muscle origin
Functional electrical skeletal muscle stimulation procedures
Mastoid myoplasty
Shortening of tendon or muscle
Maintenance of functional electrical stimulator in skeletal muscle
Division of muscle
Intrinsic muscle transfer
Eutrophic muscle stimulation
Release of cicatricial tether
Local muscle advancement flap
Muscle transfer
Irwin myotomy
Flexorplasty of elbow with extensor advancement
Physiatric manipulation of muscle structures
Myotenoplasty
Reattachment of muscle
Breast reconstruction with muscle or myocutaneous flap
Nodule in muscle
X-linked muscular dystrophy with limb girdle distribution
Congenital hereditary muscular dystrophy
Fluctuating muscle tone
Muscle sheath hernia
High frequency muscle fatigue
Generalized glycogen storage disease of infants
Persistent neonatal myasthenia gravis
Hypokalemic periodic paralysis
O/E - muscle mass normal
Traumatic rupture of skeletal muscle
Autosomal dominant muscular dystrophy with gene located at 5q31
Myopathy due to snake bite
Secondary myopathy
Lung disease with polymyositis
Muscular hypertonicity
Pelvic muscular dystrophy
Muscle tension pain
Myopathy due to systemic sclerosis
Beevor's sign
O/E - muscle power unequal
Polymyositis associated with autoimmune disease
Muscle atrophy
Finding of size of skeletal muscle
Idiopathic myoglobinuria
Muscle spasticity of spinal origin
Myoclonus epilepsy AND ragged red fibers
Myopathy in acromegaly
Congenital muscular hypertrophy-cerebral syndrome
Alcohol myopathy
Myopathy due to disseminated lupus erythematosus
Recumbency cramps
Nutritional myopathy
Trichinosis myositis
Autoimmune inflammation of skeletal muscle
Ullrich congenital muscular dystrophy
Skeletal muscle problem
Secondary fibrositis
Dermatomyositis
Dermatomyositis sine myositis
Spastic paraparesis
Drug-induced polymyositis
Mitochondrial-lipid-glycogen storage myopathy
Infective myositis
Myopathy with type I hypotrophy
Muscle ecchymosis
Reunion-Indiana Amish type muscular dystrophy
Pseudomyopathic myasthenia
Inclusion body myositis
Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
Visible muscle contraction only
Fungal myositis
Myopathy secondary to deficiency of selenium and/or vitamin E
Cogwheel muscle rigidity
Exertional rhabdomyolysis
Limb-girdle muscular dystrophy
Decorticate rigidity
Infantile myotonia
Emery-Dreifuss muscular dystrophy
Weakness present
Distal muscular dystrophy with adult onset
Pyramidal type muscle weakness
Benign monomelic amyotrophy
Finding of power of skeletal muscle
Intramuscular hematoma
Fibrositis
Glycogen storage disease, type V
Myokymia, hyperhidrosis, impaired muscle relaxation syndrome
Non-traumatic rhabdomyolysis
Viral myalgia
Traumatic injury of skeletal muscle
Muscle movement against resistance incomplete
Ji muscular dystrophy
Oculocraniosomatic syndrome
Myositis in sarcoidosis
Central core disease
Weakness of limb
Duchenne muscular dystrophy
Muscle cachexia
Fukuyama congenital muscular dystrophy
Autosomal recessive muscular dystrophy not predominantly limb girdle
Juvenile or adult myasthenia gravis
X-linked muscular dystrophy with abnormal dystrophin
Megaconial myopathy
Congenital myotonia, autosomal recessive form
Lower limb spasticity
Shoulder girdle weakness
Talc granuloma of muscle
Decerebrate rigidity
O/E - muscle atrophy present
Myoglobinuria following ingestion of eel
Late onset proximal muscular dystrophy with dysarthria
Floppy infant syndrome
Bovine eosinophilic myositis
Myasthenia gravis associated with thymoma
Drug-induced myopathy
Parasitic myositis
Myopathy due to Sjögren's disease
Facioscapulohumeral muscular dystrophy
Denervation atrophy of tongue
O/E - muscle power absent
Menopausal muscular dystrophy syndrome
Congenital anomaly of skeletal muscle
Complete bilateral paresis
Débré-Sémélaigne's syndrome
Severe x-linked myotubular myopathy
Enlargement of skeletal muscle
Myopathy due to polyarteritis nodosa
Familial periodic paralysis
O/E - muscle rigid-clasp knife
Low frequency muscle fatigue
Westphal disease
Full thickness burn involving muscle
Eichsfeld type congenital muscular dystrophy
Toxocariasis myositis
O/E - rigid muscle
Purulent myositis
Dermatomyositis with malignant disease
Equine polysaccharide storage myopathy
Benign congenital myopathy
Stringhalt
Sclerodermatomyositis
Partial thenar atrophy
Congenital myopathy with fiber type disproportion
Congenital muscular dystrophy
Muscle pain
Spinal hemiparesis
Pseudoparalysis
Eosinophilic myositis
Slow channel syndrome
Syphilis of muscle
Pelagic paralysis
Dancing doberman disease
Insufficient power to move joint
Diastasis of muscle
Muscle fatigue
Erb's muscular dystrophy
Muscular rheumatism
Protozoal myositis
Muscle contracture absent
Muscle power unequal
Neonatal neuromuscular disorder
Familial paroxysmal rhabdomyolysis
Mitochondrial myopathy
Drug-induced myasthenia
Muscle rigidity
Accessory skeletal muscle
Hereditary myopathy limited to females
Multi-core congenital myopathy
Isaacs syndrome
Charcot-Marie-Tooth disease, type IC
Endocrine myopathy
O/E - muscle contracture
Congenital absence of skeletal muscle
Merosin deficient congenital muscular dystrophy
Scapulohumeral muscular dystrophy
Intermediate X-linked muscular dystrophy
Infectious disorder of muscle
Disuse muscle atrophy
Neonatal hypotonia
Tropical pyomyositis
Peripheral muscle fatigue
Periodic paralysis II
Form of muscle
Paraneoplastic myositis
Pelvic girdle weakness
Chloroquine myopathy
Lipid storage myopathy
Diabetic amyotrophy
Generalized myasthenia
Generalized neuromuscular exhaustion syndrome
Disorder of muscle graft
O/E - muscle tone spastic
Repetitive strain injury
Acute sarcoid polymyositis
Skeletal muscle size normal
Tick paralysis
Lethal neonatal spasticity
O/E - muscle rigid - cogwheel
Focal nodular myositis
Fasciculation of tongue
Hutterite type of muscular dystrophy
Skeletal muscle tender
Pseudohypertrophy of muscle
Childhood type dermatomyositis
Muscle eye brain disease
Eosinophilic myopathy
Familial normokalemic periodic paralysis
Spastic paresis
Congenital myopathy with uniform fiber type
Muscle tone atonic
Myopathy in Cushing's disease
Mixed congenital myopathy
Polymyositis
Putative defect in acetylcholine synthesis or packaging
Amyotrophy due to herpes zoster
Quail myopathy of Lesbos
Cestode myositis
Rupture of skeletal muscle
Proliferative myositis
Bathing cramp
Tenderness at muscle insertion
Injuries of muscles and tendons involving multiple body regions
Distal muscular dystrophy
Adult onset dermatomyositis
Non dystrophic myotonia
Muscle contracture
Congenital myotonia, autosomal dominant form
Bilateral paresis
O/E - muscle mass
Coxsackie muscle infection
Canine eosinophilic myositis
Autosomal recessive muscular dystrophy with limb girdle distribution
Atrophic myositis
Skeletal muscle power problem
Myotubular myopathy with type I atrophy
Familial infantile myasthenia
Generalized myokymia
Polymyalgia
Autosomal dominant muscular dystrophy not predominantly limb girdle
Central muscle fatigue
Amyotonia congenita
Muscle irritability
Walker-Warburg congenital muscular dystrophy
Fibromyositis
Charcot-Marie-Tooth disease, type II
Mitochondrial encephalomyopathy
Distal muscle weakness
Charcot-Marie-Tooth disease, type IA
Spasticity
Myotubular myopathy
Swelling of skeletal muscle
Inappropriate firing of muscle
Proximal myopathy
Human immunodeficiency virus myopathy
Infective myositis-forearm
O/E- quadriceps muscle wasting
Neonatal myasthenia gravis
Myopathy in myasthenia gravis
Intermuscular hematoma
March myoglobinuria
Stress-induced muscle tension
Finding of arrangement of skeletal muscle
Progressive myositis ossificans
Fibrositis and nodular fasciitis
Neurological muscle weakness
Stomach cramps
Glycogen storage disease, muscular form
Eosinophilia-myalgia syndrome from tryptophan
Adult onset autosomal recessive muscular dystrophy with normal dystrophin
Zebra body myopathy
Myopathy in hyperparathyroidism
Muscle tension
Hemihypertrophy of muscle
Idiopathic polymyositis
Interstitial myositis
Neuralgic amyotrophy
Myopathy with cytoplasmic inclusions
Paramyotonia congenita
O/E - muscle power
Equine rhabdomyolysis
Pharyngeal paresis
Heat cramp
Porcine stress syndrome
Juvenile myopathy AND lactate acidosis
Movement with gravity eliminated
Adult type dermatomyositis
Congenital end-plate acetylcholinesterase deficiency
Lead pipe muscle rigidity
Denervation atrophy of muscle
Cysticercosis myositis
Thyrotoxic periodic paralysis
Failure of muscle graft
Severe childhood autosomal recessive muscular dystrophy
Muscle strain
Fibrositis of neck
Scapuloperoneal muscular dystrophy
Muscular dystrophy
Flaccidity - muscle
Abdominal weakness
No active muscle contraction
Minimal change myopathy
Familial hyperkalemic periodic paralysis
Finding of sensation of skeletal muscle
Benign congenital hypotonia
Fingerprint myopathy
Severe systemic illness-induced skeletal muscle wasting
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
Mechanical complication of muscle graft
Amyotrophy due to type 1 diabetes mellitus
O/E - muscle contraction
Acetylcholine resynthesis deficiency
Muscle weakness
Eosinophilia myalgia syndrome
Amyotrophy due to type 2 diabetes mellitus
Benign scapuloperoneal muscular dystrophy
Reduction of bulk of muscle
Muscle-eye-brain disease, congenital muscular dystrophy
Extension contracture of muscle
Myalgia/myositis - multiple
Weakness of distal arms and legs
Congenital myotonic dystrophy
Fukuhara syndrome
Upper limb spasticity
Hypothyroid myopathy
Eaton-Lambert syndrome
O/E - muscular irritability
Proximal muscle weakness
Reducing-body myopathy
Traumatic rhabdomyolysis
Antibiotic-induced neuromuscular blocking
Lesion of skeletal muscle structure
Hypoplasia of muscle
Muscular dystrophy not predominantly limb girdle in distribution
Drug-induced dermatomyositis
Myotonia acquisita
Myasthenia gravis
Main en griffe
Myopathy in Addison's disease
O/E - muscle tone atonic
O/E - paresis (weakness)
Finding of measures of skeletal muscle
Myopathy in hypoparathyroidism
Luft's hypermetabolic myopathy
Steroid-induced myopathy
Steinert myotonic dystrophy syndrome
Glycogen storage disease, type VII
Penicillamine-induced myasthenia
Myopathy due to rheumatoid arthritis
O/E - muscle power normal
Idiopathic dermatomyositis
Myopathy in hypopituitarism
Hereditary progressive muscular dystrophy
Primary fibrositis
Myositis
Nemaline myopathy
Myopathy with tubular aggregates
Disorder of skeletal muscle
Laryngeal paresis
Primary familial amyloid myopathy
Partial bilateral paresis
Movement against gravity
Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency
Myomalacia
Myedema
Cramp
Pain on movement of skeletal muscle
Glycogen storage disease type III
Muscle AMP deaminase deficiency
Hydatidosis myositis
Western type of congenital muscular dystrophy
Fibrositis arm
Nemaline myopathy, early onset type
Infection of muscle graft
Diffuse rigidity
Paraplegic immobility syndrome
Autosomal recessive centronuclear myopathy
Diffuse muscle tenderness
Severe autosomal recessive muscular dystrophy of childhood - North African type
Charcot-Marie-Tooth disease, type I
Congenital myasthenia
Triglyceride storage disease with ichthyosis
O/E - extension contracture
Primary fibromyalgia syndrome
Severe scapuloperoneal muscular dystrophy with cardiomyopathy
Myotonia due to drug
Roussy-Lévy syndrome
Poikilodermatomyositis
Myotonia levior
Distal muscular dystrophy, Miyoshi type
Flexion contracture of muscle
Traumatic division of muscle
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
Glycogen synthase deficiency
Haff syndrome
Hereditary myopathy associated with hydrocephalus
Viral myositis
Myokymia
Manifesting female carrier of X-linked muscular dystrophy
Maxillary myositis
Protein deficiency myopathy
Muscle fasciculation
Toxic myopathy
Grade of muscle power - finding
Ophthalmoplegia plus syndrome
Ischemic infarction of muscle
O/E - muscular fasciculation
Muscular dystrophy-deafmutism syndrome
Floppy muscles
X-linked muscular dystrophy not predominantly limb girdle
Charcot-Marie-Tooth disease, type IB
Deposition in skeletal muscle
Glycogen storage disease, type IV
Muscular dystrophy with predominantly proximal limb girdle distribution
Sarcotubular myopathy
Myasthenia gravis, adult form
Distal muscular dystrophy with juvenile onset
Enthesitis
Ocular muscular dystrophy
Amyotrophia congenita
Chronic sarcoid myopathy
Myopathy in osteomalacia
O/E - muscle tension
Myasthenic crisis
Autosomal dominant muscular dystrophy with limb girdle distribution
Sarcoid myopathy
Carcinomatous myopathic syndrome
Polymyositis with malignant disease
O/E - muscle power reduced
Pseudoparalysis due to generalized arthritis
Oculopharyngeal muscular dystrophy
Transient neonatal myasthenia
Congenital myopathy with abnormal subcellular organelles
Muscle hypertrophy
Charcot-Marie-Tooth disease
Hereditary myositis ossificans
Primary sporadic amyloid myopathy
Eosinophilic polymyositis
Spastic paralysis
Finding of appearance of skeletal muscle
Movement against resistance
Subjective muscle weakness
Amyloid myopathy
Poor muscle tone
Combined malformation of central nervous system and skeletal muscle
Abnormality of synaptic vesicles
Charleyhorse
Nemaline myopathy, late onset type
Rotator cuff impingement syndrome
Skeletal muscle normal
Named sign of skeletal muscle
Pseudocholinesterase deficiency
Nematode myositis
Becker muscular dystrophy
Ischemic muscular atrophy
Myofibrosis
Congenital muscular dystrophy with arthrogryposis multiplex congenita
Clasp knife like increase in tone
Metabolic myopathy
Myopathy with abnormality of histochemical fiber type
Spinal paraparesis
Hemorrhage of muscle
O/E-muscle hypertrophy present
Paresis of lower extremity
Autosomal recessive muscular dystrophy with gene located at 15q
Muscle tender point
Congenital and developmental myasthenia
Myoneural disorder
Congenital end-plate acetylcholine receptor deficiency
Benign congenital muscular dystrophy with finger flexion contractures
Thyrotoxic myopathy
Palatal paresis
Intramuscular contusion
Toxic neuromuscular junction disorder
Myotonic disorder
Chronic myopathy with hypocalcemia and hypophosphatemia
Genetically determined myasthenia
Potassium depletion myopathy
Rhabdomyolysis
X-linked limb girdle muscular dystrophy with normal dystrophin
Benign acute myositis
Hand muscle weakness
Familial hypokalemic periodic paralysis
Congenital nonprogressive myopathy with Moebius and Robin sequences
Immobility syndrome
Myasthenia gravis, juvenile form
MRC grade - muscle power - finding
Benign scapuloperoneal muscular dystrophy with cardiomyopathy
Intramuscular injection of methylprednisolone
Intramuscular infiltration of local anesthetic
Intramuscular gold therapy
Intramuscular infiltration
Intramuscular hormone therapy
Insertion of skeletal muscle stimulator
Intramuscular drug injection
Drainage of muscle
Intramuscular injection of Methotrexate
Intramuscular infiltration of botulinum toxin
Injection of muscle for local action
Intramuscular injection of vitamin B12
Intramuscular injection
Removal of skeletal muscle stimulator
Intramuscular immunotherapy
Drainage of intramuscular hematoma
Intramuscular injection of betamethasone
Intramuscular infiltration of local anesthetic and steroid
Intramuscular injection for local action
Intramuscular chemotherapy
Intramuscular infiltration of neurolytic substance
Intramuscular infiltration of steroid
Medication administration: intramuscular
Drainage of intramuscular abscess
Removal of foreign body from muscle
Intramuscular calcitonin therapy
Intramuscular steroid therapy
Intramuscular antibiotic therapy
Skeletal muscle system structure
Soft tissues
Muscle structure
1
Entire skeletal muscle system
Edrophonium chloride test for myasthenia gravis
Manual muscle-testing of total body including hands
Extremity testing for strength, dexterity or stamina
Range of motion measurements and report for hand
Edrophonium chloride test with electromyographic recording
Operation on skeletal muscle
Manual muscle-testing of total body excluding hands
Strayer procedure
Manual testing of muscle function
Gastrocnemius recession
Manual muscle-testing with total evaluation of body
Electrical muscle-testing
Range of motion testing
Muscle-testing with torque curves during isometric and isokinetic exercise
Muscle function study
Body Part, Organ, or Organ Component
Tissue
T-D0684
Skeletal muscle cytologic material
Skeletal muscle specimen
Specimen from skeletal muscle obtained by biopsy
T023
T024
C1331262
C0242692