AutoICD API

M62.89

Billable

Other specified disorders of muscle

Other specified disorders of muscle

Status

Billable / Specific

Block

M60-M63

Parent Code

M62.8

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)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(5)
M62.81

Muscle weakness (generalized)

BillableM62.82

Rhabdomyolysis

BillableM62.83

Muscle spasm

M62.84

Sarcopenia

BillableM62.85

Dysfunction of the multifidus muscles, lumbar region

Billable
Also Known As / Clinical Terms(313)

SNOMED CT

UMLS

Clinical Terms

  • Increased muscle tone
  • Hypotonia of muscles of mouth region
  • Hemorrhage of muscle
  • Increased muscle tone - right side more than left side
  • Episodic muscular flaccidity
  • Hereditary continuous muscle fiber activity
  • Hypertonia
  • Paraspinal muscle hypertrophy
  • Large skeletal muscle
  • H1-4-related neurodevelopmental disorder
  • Increased bulk of muscle
  • Myotonia due to cold exposure
  • Velopharyngeal insufficiency
  • Myotonia acquisita
  • Hypertrophy of left masseter muscle
  • Hypertrophy of muscle of right lower limb
  • Hypertrophy of muscle of right upper limb
  • Hypertrophy of bilateral masseter muscles
  • Protective co-contraction of masticatory muscles
  • Generalized myokymia
  • Subaponeurotic haemorrhage
  • Peripheral muscle fatigue
  • Haemorrhage of muscle
  • Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome
  • Observation of size of skeletal muscle
  • Débré-Sémélaigne syndrome
  • Fatal pontocerebellar hypoplasia, hypotonia, respiratory distress syndrome
  • Muscle tiredness
  • Spontaneous electromyography activity
  • Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation
  • Abnormally decreased muscle contraction
  • Hypertrophy of muscle of upper limb
  • Inappropriate firing of muscle
  • Subgaleal haemorrhage
  • Herniation of lumbar muscles
  • Microcephaly, intellectual disability, sensorineural deafness, epilepsy, abnormal muscle tone syndrome
  • Muscle fibrillation
  • Episodic hypotonia
  • Muscle hypertonia
  • Talma's disease
  • Hereditary cerebellar atrophy
  • Epicranial subaponeurotic hemorrhage
  • Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome
  • Bilateral hypertrophy of masseter muscles
  • Exercise induced muscle fatigue
  • Hypertrophy of both masseter muscles
  • Tight muscle
  • Flaccidity of muscle of upper limb
  • Hypertrophic mitochondrial cardiomyopathy
  • Skeletal muscle hypertrophy
  • Epicranial subaponeurotic haemorrhage
  • Infantile axial hypotonia
  • Masticatory muscle hypertrophy
  • Structural velopharyngeal impairment
  • Severe hypertrophy of skeletal muscle
  • Muscle fatigue
  • Asymmetric muscle tone
  • Hypertrophy of erector spinae muscle
  • Tonic spasm of muscle
  • Episodic flaccid muscle
  • Floppy infant
  • Congenital radioulnar synostosis
  • Appendicular hypotonia
  • Hypertrophy of right masseter muscle
  • Increased muscle tone - left side more than right side
  • Hemihypertrophy of skeletal muscle
  • Oral hypotonia
  • Quadratus lumborum syndrome
  • Muscle (sheath) hernia
  • High muscle tone
  • Muscles tire easily
  • X-linked intellectual disability, hypotonia, movement disorder syndrome
  • Myofibrosis
  • Degenerative disorder of muscle
  • Muscle power unequal
  • Reinnervation
  • Reduction of bulk of muscle
  • Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
  • Radioulnar synostosis with developmental delay and hypotonia syndrome
  • High frequency muscle fatigue
  • Muscle tone asymmetric
  • Hypertrophy of muscle of thigh
  • Fluctuating muscle tone
  • Flaccidity of muscle
  • Facial hypotonia
  • Hypertrophy of muscle of left upper limb
  • Fatal pontocerebellar hypoplasia, hypotonia, respiratory insufficiency syndrome
  • Floppy baby
  • Hypertrophy of muscle of upper arm
  • Protective splinting of masticatory muscles
  • Hypertrophy of muscle of left lower limb
  • Débré-Sémélaigne's syndrome
  • Myotonus
  • Incomplete closure of velopharyngeal apparatus due to anatomical abnormality
  • Respiratory insufficiency syndrome of newborn
  • Cerebellar ataxia, brain abnormalities, cardiac conduction defects syndrome
  • Episodic floppy muscle
  • Lethal pontocerebellar hypoplasia, hypotonia, respiratory insufficiency syndrome
  • Muscle asynchronous firing potential
  • Nodule in muscle
  • Floppy infant syndrome
  • Hypertrophy of muscle of lower limb
  • Flaccidity of muscle of lower limb
  • Myomalacia
  • Hypertrophy of muscle of neck
  • Neonatal neuromuscular disorder
  • Rahman syndrome
  • Skeletal muscle problem
  • Neonatal hypotonia
  • Hereditary continuous muscle fibre activity
  • Neurodevelopmental delay, hypotonia, cerebellar atrophy, cardiac conduction defects syndrome
  • Hemihypertrophy of muscle
  • X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome
  • Skeletal muscle power problem
  • Spontaneous EMG activity
  • Exertional muscle fatigue
  • Observation of appearance of skeletal muscle
  • Floppy muscle
  • Low frequency muscle fatigue
  • Flaccid muscle
  • Generalised hypertrophy of skeletal muscle
  • Generalized hypertrophy of skeletal muscle
  • Muscle irritability
  • Generalised myokymia
  • Subaponeurotic hemorrhage
  • Myokymia, hyperhidrosis, impaired muscle relaxation syndrome
  • Myotonia
  • Reduction of bulk of skeletal muscle
  • Hypertrophy of muscle of shoulder joint
  • Severe muscular hypertrophy
  • Finding of appearance of skeletal muscle
  • Hypotonia of axial muscles occurring in infancy
  • Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome
  • Episodic flaccidity of muscle
  • Muscle hypertrophy
  • Hypertrophy of muscle of calf
  • Debre-Semelaigne's syndrome
  • Central muscle fatigue
  • PPP2R5D-related intellectual disability
  • Hypotonia of muscle of face
  • Acquired hypotonia
  • Hypertrophy of masseter muscle
  • Hypertrophy of muscles of mastication
  • Enlargement of skeletal muscle
  • Finding of size of skeletal muscle
  • Hypertrophy of muscle of forearm
  • Muscular flaccidity
  • Subgaleal hemorrhage
  • Der Kaloustian McIntosh Silver syndrome
  • X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behaviour syndrome
  • Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome
  • Muscular steatosis
  • Hernia of muscle through fascia of lower leg
  • Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation
  • Deposition in skeletal muscle
  • Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome
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.

How does M62.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified disorders of muscle affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of M62.89?

There is no direct ICD-11 mapping available for M62.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.