M62.89
BillableOther specified disorders of muscle
Other specified disorders of muscle
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Muscle (sheath) hernia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- dermatopolymyositis (M33.-)
- myopathy in amyloidosis (E85.-)
- myopathy in polyarteritis nodosa (M30.0)
- myopathy in rheumatoid arthritis (M05.32)
- myopathy in scleroderma (M34.-)
- myopathy in Sjögren's syndrome (M35.03)
- myopathy in systemic lupus erythematosus (M32.-)
- alcoholic myopathy (G72.1)
- cramp and spasm (R25.2)
- drug-induced myopathy (G72.0)
- myalgia (M79.1-)
- stiff-man syndrome (G25.82)
Excludes 2
Conditions not included here, but the patient may have both
- arthropathic psoriasis (L40.5-)
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- compartment syndrome (traumatic) (T79.A-)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- muscular dystrophies and myopathies (G71-G72)
- nontraumatic hematoma of muscle (M79.81)
Also Known As / Clinical Terms
SNOMED CT
- Myotonia3434004
- Myotonus3434004
- Tonic spasm of muscle3434004
- Peripheral muscle fatigue17099003
- Muscle asynchronous firing potential28755004
- Muscular steatosis40725000
- Muscle fibrillation41405005
- Debre-Semelaigne's syndrome41505007
- Débré-Sémélaigne syndrome41505007
- Débré-Sémélaigne's syndrome41505007
- High muscle tone56731001
- Hypertonia56731001
- Increased muscle tone56731001
- Muscle hypertonia56731001
- Tight muscle56731001
- Reinnervation63514004
- Low frequency muscle fatigue65927007
- Myomalacia77897003
- Central muscle fatigue79117005
- High frequency muscle fatigue79215008
- Muscle fatigue80449002
- Muscle tiredness80449002
- Muscles tire easily80449002
- Myofibrosis83049007
- Myotonia acquisita85034001
- Talma's disease85034001
- Haemorrhage of muscle95422003
- Hemorrhage of muscle95422003
- Abnormally decreased muscle contraction102543005
- Protective co-contraction of masticatory muscles109665002
- Protective splinting of masticatory muscles109665002
- Flaccid muscle186611004
- Flaccidity of muscle186611004
- Floppy muscle186611004
- Muscular flaccidity186611004
- Inappropriate firing of muscle203086008
- Floppy baby205294008
- Floppy infant205294008
- Floppy infant syndrome205294008
- Neonatal hypotonia205294008
- Incomplete closure of velopharyngeal apparatus due to anatomical abnormality229726002
- Structural velopharyngeal impairment229726002
- Velopharyngeal insufficiency229726002
- Quadratus lumborum syndrome247370006
- Herniation of lumbar muscles249728005
- Muscle hypertrophy249829006
- Skeletal muscle hypertrophy249829006
- Hemihypertrophy of muscle249831002
- Hemihypertrophy of skeletal muscle249831002
- Muscle power unequal249947004
- Fluctuating muscle tone250076001
- Generalised myokymia250079008
- Generalized myokymia250079008
- Myokymia, hyperhidrosis, impaired muscle relaxation syndrome250081005
- Spontaneous EMG activity251525000
- Spontaneous electromyography activity251525000
- Muscle irritability271697007
- Respiratory insufficiency syndrome of newborn276536005
- Epicranial subaponeurotic haemorrhage276622005
- Epicranial subaponeurotic hemorrhage276622005
- Subaponeurotic haemorrhage276622005
- Subaponeurotic hemorrhage276622005
- Subgaleal haemorrhage276622005
- Subgaleal hemorrhage276622005
- Finding of appearance of skeletal muscle298272002
- Observation of appearance of skeletal muscle298272002
- Finding of size of skeletal muscle298273007
- Observation of size of skeletal muscle298273007
- Enlargement of skeletal muscle298274001
- Increased bulk of muscle298274001
- Large skeletal muscle298274001
- Deposition in skeletal muscle298278003
- Nodule in muscle298279006
- Skeletal muscle power problem298286003
- Skeletal muscle problem298301007
- Reduction of bulk of muscle300043006
- Reduction of bulk of skeletal muscle300043006
- Degenerative disorder of muscle363058009
- Neonatal neuromuscular disorder363222009
- Asymmetric muscle tone406146007
- Muscle tone asymmetric406146007
- Increased muscle tone - left side more than right side422966009
- Increased muscle tone - right side more than left side424676008
- Flaccidity of muscle of lower limb449909007
- Flaccidity of muscle of upper limb449910002
- Hypertrophic mitochondrial cardiomyopathy472316006
- Hypertrophy of muscles of mastication699458005
- Masticatory muscle hypertrophy699458005
- Hypertrophy of masseter muscle699649006
- Acquired hypotonia704200007
- Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome718713000
- X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome719157002
- X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behaviour syndrome719157002
- Der Kaloustian McIntosh Silver syndrome721883006
- Radioulnar synostosis with developmental delay and hypotonia syndrome721883006
- Hernia of muscle through fascia of lower leg726674004
- Exercise induced muscle fatigue1119506007
- Exertional muscle fatigue1119506007
- Appendicular hypotonia1137379000
- Myotonia due to cold exposure1137383000
- Episodic hypotonia1137384006
- Facial hypotonia1137385007
- Hypotonia of muscle of face1137385007
- Hypotonia of axial muscles occurring in infancy1137387004
- Infantile axial hypotonia1137387004
- Hypotonia of muscles of mouth region1137399006
- Oral hypotonia1137399006
- Episodic flaccid muscle1137496003
- Episodic flaccidity of muscle1137496003
- Episodic floppy muscle1137496003
- Episodic muscular flaccidity1137496003
- Hypertrophy of muscle of calf1142246005
- Hypertrophy of muscle of forearm1142248006
- Generalised hypertrophy of skeletal muscle1142249003
- Generalized hypertrophy of skeletal muscle1142249003
- Hypertrophy of muscle of left lower limb1142250003
- Hypertrophy of muscle of right lower limb1142251004
- Hypertrophy of muscle of left upper limb1142252006
- Hypertrophy of muscle of right upper limb1142253001
- Severe hypertrophy of skeletal muscle1142259002
- Severe muscular hypertrophy1142259002
- Hypertrophy of muscle of lower limb1142261006
- Hypertrophy of muscle of neck1142262004
- Hypertrophy of erector spinae muscle1142263009
- Paraspinal muscle hypertrophy1142263009
- Hypertrophy of muscle of upper arm1142264003
- Hypertrophy of muscle of shoulder joint1142266001
- Hypertrophy of muscle of thigh1142267005
- Hypertrophy of muscle of upper limb1142268000
- Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome1172696009
- Hereditary continuous muscle fiber activity1231178006
- Hereditary continuous muscle fibre activity1231178006
- Microcephaly, intellectual disability, sensorineural deafness, epilepsy, abnormal muscle tone syndrome1254651003
- Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome1254651003
- Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome1254652005
- Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome1254652005
- PPP2R5D-related intellectual disability1254652005
- X-linked intellectual disability, hypotonia, movement disorder syndrome1254654006
- Congenital radioulnar synostosis1268409009
- Cerebellar ataxia, brain abnormalities, cardiac conduction defects syndrome1303586006
- Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome1303586006
- Neurodevelopmental delay, hypotonia, cerebellar atrophy, cardiac conduction defects syndrome1303586006
- Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation1304277005
- Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation1304277005
- H1-4-related neurodevelopmental disorder1304277005
- Rahman syndrome1304277005
- Fatal pontocerebellar hypoplasia, hypotonia, respiratory distress syndrome1362022003
- Fatal pontocerebellar hypoplasia, hypotonia, respiratory insufficiency syndrome1362022003
- Lethal pontocerebellar hypoplasia, hypotonia, respiratory insufficiency syndrome1362022003
- Bilateral hypertrophy of masseter muscles15747881000119103
- Hypertrophy of bilateral masseter muscles15747881000119103
- Hypertrophy of both masseter muscles15747881000119103
- Hereditary cerebellar atrophy431641000124107
- Hypertrophy of left masseter muscle15747841000119108
- Hypertrophy of right masseter muscle15747801000119106
Frequently Asked Questions
What is the ICD-10 code for other specified disorders of muscle?
The ICD-10-CM code for other specified disorders of muscle is M62.89. The full clinical description is "Other specified disorders of muscle". M62.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M62.89 mean?
ICD-10-CM code M62.89 represents "Other specified disorders of muscle". It is classified under Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue and is a billable/specific code that can be used on a claim.
Is M62.89 a billable code?
Yes, M62.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M62.89 in?
M62.89 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M62.89?
M62.89 has Excludes1 notes indicating codes that cannot be used together with it, including: dermatopolymyositis (M33.-); myopathy in amyloidosis (E85.-); myopathy in polyarteritis nodosa (M30.0); and 9 more.
What SNOMED CT codes does M62.89 map to?
M62.89 maps to 93 SNOMED CT concepts: 102543005, 704200007, 1137379000, 406146007, 1304277005, and 88 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M62.89?
M62.89 is linked to 2 UMLS Concept Unique Identifiers: C0343258, C0029741. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.