Disorder of skeletal muscle   75047002

SNOMED CT code


SNOMED code75047002
nameDisorder of skeletal muscle
statusactive
date introduced2002-01-31
fully specified name(s)Disorder of skeletal muscle (disorder)
synonyms
  • Disease of skeletal muscle
  • Disorder of skeletal muscle
attributes - group1
Finding siteSkeletal muscle structure   127954009
parents
children
  • [X]Disorder of muscle, unspecified   203845002  removed: 2009-01-31
  • [X]Muscle wasting and atrophy, not elsewhere classified   203838002  removed: 2009-01-31
  • [X]Myositis in protozoal and parasitic infections classified elsewhere   203841006  removed: 2009-01-31
  • [X]Other disorders of muscle in diseases classified elsewhere   203844003  removed: 2009-01-31
  • [X]Other primary disorders of muscles   194533009  removed: 2009-01-31
  • [X]Other rupture of muscle (nontraumatic)   203837007  removed: 2009-01-31
  • [X]Other specified disorders of muscle   203839005  removed: 2009-01-31
  • Acquired hypotonia   704200007
  • Allan-Herndon-Dudley syndrome   702327009
  • Andersen Tawil syndrome   422348008
  • Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis   829973009
  • Autosomal recessive lower motor neuron disease with childhood onset   771302009
  • Benign congenital hypotonia   240080003
  • Borderline velopharyngeal adequacy   10998911000119105
  • Brody myopathy   703530005
  • Cap myopathy   703532002
  • Caveolin 3 related distal myopathy   711265009
  • Combined oxidative phosphorylation defect type 30   1172841001
  • Complete rectal prolapse with displacement of anal sphincter   43411001
  • Congenital anomaly of skeletal muscle   89886004
  • Congenital contracture of limbs and face, hypotonia, developmental delay syndrome   1255322002
  • Congenital laryngeal abductor palsy   232442001
  • Congenital laryngeal adductor palsy   232443006
  • Congenital spastic foot   230779009
  • Cricopharyngeal disorder   235631007
  • Cystinuria, type 1   37183000
  • Denervation atrophy of muscle   74035001
  • Denervation of external urethral sphincter   699294006
  • Deposition in skeletal muscle   298278003
  • Disorder of diaphragm   48475001
  • Disorder of extraocular muscle   128603005
  • Disorder of muscle graft   271978005
  • Disuse atrophy   86542002  removed: 2006-01-31
  • Drug-induced myopathy   240101000
  • Débré-Sémélaigne's syndrome   41505007
  • Edema of skeletal muscle   277374006
  • Eosinophilia myalgia syndrome   95416007
  • Eosinophilic myopathy   76762001
  • Equine rhabdomyolysis   24919008  removed: 2014-01-31
  • Fibrositis   56557000
  • Fingerprint myopathy   23820006
  • Glycogen storage disease due to lactate dehydrogenase deficiency   1186809004
  • Glycogen synthase deficiency   237964009
  • GNAO1-related developmental delay, seizures, movement disorder spectrum   1281842000
  • Hemorrhage of muscle   95422003
  • Hereditary continuous muscle fiber activity   1231178006
  • Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome   771306007
  • Hereditary myopathy associated with hydrocephalus   53387004
  • Hernia of muscle through fascia of lower leg   726674004
  • Herniation of lumbar muscles   249728005
  • Hoffman syndrome   716338001
  • Hypertrophy of masseter muscle   699649006
  • Hypertrophy of orbicularis oculi muscle   246840002
  • Hypoplasia of muscle   205530002
  • Immobility syndrome   203041005
  • Incomplete closure of velopharyngeal apparatus due to anatomical abnormality   229726002
  • Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome   1217371005
  • Infectious disorder of muscle   363163005
  • Inherited spastic paresis   16728003  removed: 2020-07-31
  • Injury of adductor muscle of thigh   726225005
  • Injury of biceps brachii muscle   724921009
  • Injury of extensor muscle at forearm level   724980007
  • Injury of flexor muscle and tendon of thumb at forearm level   212459001
  • Injury of flexor muscle of finger at forearm level   724953000
  • Injury of flexor muscle of thumb at forearm level   724944007
  • Injury of intrinsic muscle of finger   726199004
  • Injury of intrinsic muscle of foot   726322006
  • Injury of intrinsic muscle of left hand   11839531000119108
  • Injury of intrinsic muscle of right hand   11839431000119109
  • Injury of intrinsic muscle of thumb   726190000
  • Injury of muscle and tendon at forearm level   212458009
  • Injury of muscle and tendon at hip and thigh level   212467009
  • Injury of muscle at forearm level   724940003
  • Injury of muscle at shoulder level   724905004
  • Injury of muscle at upper arm level   724908002
  • Injury of muscle of head   725003001
  • Injury of muscle of hip   726216004
  • Injury of muscle of left upper arm   11780521000119105
  • Injury of muscle of lower leg   880083009
  • Injury of muscle of neck   725013009
  • Injury of muscle of right upper arm   11780481000119105
  • Injury of muscle of rotator cuff   733227000
  • Injury of muscle of thigh   1252752000
  • Injury of muscle of trunk   726331006
  • Injury of triceps brachii muscle   724930001
  • Intellectual disability, cataract, calcified pinna, myopathy syndrome   726709001
  • Intellectual disability, epilepsy, extrapyramidal syndrome   1187210007
  • Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome   1254652005
  • Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome   1208746001
  • Isaacs syndrome   80138003
  • Laryngeal dystonia   3331000119108
  • Laryngeal spasm   42006002  removed: 2004-01-31
  • Left shoulder skeletal muscle injury   11780841000119102
  • Lesion of skeletal muscle   298277008
  • Lethal neonatal spasticity   54364001  removed: 2022-02-28
  • Lethal neonatal spasticity, epileptic encephalopathy syndrome   1197587003
  • Metabolic myopathy   26111005
  • Microcephalus, brain defect, spasticity, hypernatremia syndrome   770655004
  • Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome   1254651003
  • Minimal change myopathy   76492009
  • Multiple congenital anomalies, hypotonia, seizures syndrome   785303004
  • Muscle atrophy   88092000
  • Muscle cachexia   240128005
  • Muscle damage NOS   240045002  removed: 2010-01-31
  • Muscle paralysis due to and following neuromuscular blockade   823019007
  • Muscle paresis due to and following neuromuscular blockade   823018004
  • Muscle spasm of head and/or neck   95418008
  • Muscular dystrophies and other myopathies   193219004  removed: 2008-07-31
  • Muscular dystrophy   73297009
  • Muscular hypertonicity   41581000
  • Muscular rheumatism   203102006
  • Myalgia and myositis unspecified   203108005  removed: 2010-01-31
  • Myoclonus of tensor tympani muscle   427789001
  • Myofascial pain syndrome   726531007
  • Myofibrillar myopathy   699269005
  • Myokymia, hyperhidrosis, impaired muscle relaxation syndrome   250081005
  • Myomalacia   77897003
  • Myoneural disorder   257277002
  • Myopathy   52794005  removed: 2002-07-31
  • Myopathy due to calsequestrin and SERCA1 protein overload   724095006
  • Myopathy due to disseminated lupus erythematosus   193248005
  • Myopathy due to polyarteritis nodosa   193249002
  • Myopathy due to rheumatoid arthritis   193250002
  • Myopathy due to scleroderma   193252005
  • Myopathy due to Sjögren's disease   193253000
  • Myopathy or muscular dystrophy NOS   193261005  removed: 2010-01-31
  • Myopathy with deficiency of iron-sulfur cluster assembly enzyme   699268002
  • Myosclerosis   763895001
  • Myosin storage myopathy   699267007
  • Myositis   26889001
  • Myotonia acquisita   85034001
  • Myotonia levior   8960007
  • Myotonic disorder   193237003
  • Nemaline myopathy   75072002
  • Ophthalmoplegia plus syndrome   77835008
  • Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome   1222655009
  • Other myopathies and muscular dystrophies   193260006  removed: 2010-01-31
  • Other specific muscle disorder   203039009  removed: 2010-01-31
  • Other specific muscle disorder NOS   203043008  removed: 2010-01-31
  • Palatal paralysis   232414003  removed: 2004-01-31
  • Palatopharyngeal incoordination   232415002
  • Paresis as late effect of poliomyelitis   138371000119104
  • Paresis of left vocal cord   1052239007
  • Paresis of right vocal cord   1052240009
  • Pelvic floor dysfunction   711263002
  • Polymyalgia   95415006
  • Proximal myopathy   193255007
  • Pseudocholinesterase deficiency   191397007  removed: 2020-01-31
  • Quadratus lumborum syndrome   247370006
  • Reducing-body myopathy   42779002
  • Rhabdomyolysis   240131006
  • Right shoulder skeletal muscle injury   11780801000119104
  • Rotator cuff impingement syndrome   359532006
  • Rotator cuff shoulder syndrome and allied disorders   202838007  removed: 2016-01-31
  • Sarcopenia   772791006
  • Secondary myopathy   60738003
  • Spastic diplegia   281411007
  • Spastic paraparesis and deafness   715504003
  • Spasticity as sequela of stroke   108691000119102
  • Stapedial myoclonus   426187002
  • Stimulation of muscle pocket as complication of implantation of automatic cardiac defibrillator   762667005
  • Stimulation of muscle pocket as complication of implantation of cardiac pacemaker   762668000
  • Tetraparesis   91327001
  • Toxic myopathy   66952001
  • Triglyceride storage disease with ichthyosis   19604005
  • Velopharyngeal dysfunction   229727006
  • Velopharyngeal mislearning   229728001
  • Weakness of extremities as sequela of stroke   92341000119107
  • Weakness of face muscles as sequela of stroke   40161000119102
  • Weakness of left facial muscle as sequela of cerebrovascular disease   15982311000119104
  • Weakness of left facial muscle due to and following non-traumatic intracerebral hemorrhage   15982431000119103
  • Weakness of right facial muscle as sequela of cerebrovascular disease   15982271000119104
  • Weakness of right facial muscle due to and following spontaneous intracerebral hemorrhage   15982191000119106
  • X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome   719157002
  • X-linked parkinsonism with spasticity syndrome   770757004
  • X-linked spasticity, intellectual disability, epilepsy syndrome   725163002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Muscle finding   106030000
      Disorder of muscle   129565002
        Disorder of skeletal muscle   75047002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    General finding of soft tissue   248402002
      Disorder of soft tissue   19660004
        Disorder of skeletal muscle   75047002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Disorder of skeletal muscle   75047002

ancestors
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