Code First Notes in Chapter 13: Diseases of the musculoskeletal system and connective tissue ICD-10-CM
A Code First note means the underlying condition named in the note is sequenced before this code. In Chapter 13 (M00-M99), notes printed in the chapter name other codes 87 times, and Code First Notes anywhere in the Tabular List name the chapter’s codes 53 times, covering 30 distinct codes, categories and ranges. Switch views to read the list either way.
Code First Notes by the code that carries the note
- M01 Direct infections of joint in infectious and parasitic diseases classified elsewhere applies to 24 codes
- M05.A Abnormal rheumatoid factor and anti-citrullinated protein antibody with rheumatoid arthritis
- toxic effects of lead and its compounds (T56.0-)
- toxic effects of lead and its compounds (T56.0-)
- M31.11 Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA]
- M34.2 Systemic sclerosis induced by drug and chemical
- M35.81 Multisystem inflammatory syndrome
- , if applicable, COVID-19 (U07.1)
- M36.0 Dermato(poly)myositis in neoplastic disease
- M36.1 Arthropathy in neoplastic disease
- M36.2 Hemophilic arthropathy
- M36.3 Arthropathy in other blood disorders
- M36.4 Arthropathy in hypersensitivity reactions classified elsewhere
- M36.8 Systemic disorders of connective tissue in other diseases classified elsewhere
- M51.A0 Intervertebral annulus fibrosus defect, lumbar region, unspecified size
- M51.A1 Intervertebral annulus fibrosus defect, small, lumbar region
- M51.A2 Intervertebral annulus fibrosus defect, large, lumbar region
- M51.A3 Intervertebral annulus fibrosus defect, lumbosacral region, unspecified size
- M51.A4 Intervertebral annulus fibrosus defect, small, lumbosacral region
- M51.A5 Intervertebral annulus fibrosus defect, large, lumbosacral region
- M62.84 Sarcopenia
- any associated slipped upper femoral epiphysis (nontraumatic) (M93.0-)
- L86 Keratoderma in diseases classified elsewhere: Reiter's disease (M02.3-)
- M05.00 Felty's syndrome, unspecified site
- M05.A Abnormal rheumatoid factor and anti-citrullinated protein antibody with rheumatoid arthritis: rheumatoid arthritis with rheumatoid factor by site, if known (M05.00 to M05.8A)
- M05.8A Other rheumatoid arthritis with rheumatoid factor of other specified site
- M05.A Abnormal rheumatoid factor and anti-citrullinated protein antibody with rheumatoid arthritis: rheumatoid arthritis with rheumatoid factor by site, if known (M05.00 to M05.8A)
- I43 Cardiomyopathy in diseases classified elsewhere: gout (M10.0-)
- G99.0 Autonomic neuropathy in diseases classified elsewhere: gout (M1A.-, M10.-)
- H22 Disorders of iris and ciliary body in diseases classified elsewhere: gout (M1A.-, M10.-)
- H62.8 Other disorders of external ear in diseases classified elsewhere: gout (M1A.-, M10.-)
- N08 Glomerular disorders in diseases classified elsewhere: gout (M1A.-, M10.-)
- N22 Calculus of urinary tract in diseases classified elsewhere: gout (M1A.-, M10.-)
- G99.0 Autonomic neuropathy in diseases classified elsewhere: gout (M1A.-, M10.-)
- H22 Disorders of iris and ciliary body in diseases classified elsewhere: gout (M1A.-, M10.-)
- H62.8 Other disorders of external ear in diseases classified elsewhere: gout (M1A.-, M10.-)
- N08 Glomerular disorders in diseases classified elsewhere: gout (M1A.-, M10.-)
- N22 Calculus of urinary tract in diseases classified elsewhere: gout (M1A.-, M10.-)
- M30.0 Polyarteritis nodosa
- F02 Dementia in other diseases classified elsewhere: polyarteritis nodosa (M30.0)
- M30-M36 Polyarteritis nodosa and related conditions to Systemic disorders of connective tissue in diseases classified elsewhere 84 codes
- J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere: systemic connective tissue disorders (M30-M36)
- M31.7 Microscopic polyangiitis
- N08 Glomerular disorders in diseases classified elsewhere: microscopic polyangiitis (M31.7)
- M32.0-M32.9 Drug-induced systemic lupus erythematosus to Systemic lupus erythematosus, unspecified 10 codes
- J84.178 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere: systemic lupus erythematosis (M32.0-M32.9)
- M32.19 Other organ or system involvement in systemic lupus erythematosus
- M34.0 Progressive systemic sclerosis
- J84.178 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere: progressive systemic sclerosis (M34.0)
- K31.84 Gastroparesis: scleroderma (M34.-)
- M35.2 Behcet's disease
- N77.0 Ulceration of vulva in diseases classified elsewhere: Behçet's disease (M35.2)
- M35.81 Multisystem inflammatory syndrome
- U09.9 Post COVID-19 condition, unspecified: multisystem inflammatory syndrome (M35.81)
- M35.9 Systemic involvement of connective tissue, unspecified
- G32.81 Cerebellar ataxia in diseases classified elsewhere: non-celiac gluten ataxia (M35.9)
- J99 Respiratory disorders in diseases classified elsewhere: ankylosing spondylitis (M45.-)
- M51.06 Intervertebral disc disorders with myelopathy, lumbar region
- M51.A0 Intervertebral annulus fibrosus defect, lumbar region, unspecified size: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.A1 Intervertebral annulus fibrosus defect, small, lumbar region: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.A2 Intervertebral annulus fibrosus defect, large, lumbar region: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.16 Intervertebral disc disorders with radiculopathy, lumbar region
- M51.A0 Intervertebral annulus fibrosus defect, lumbar region, unspecified size: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.A1 Intervertebral annulus fibrosus defect, small, lumbar region: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.A2 Intervertebral annulus fibrosus defect, large, lumbar region: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.17 Intervertebral disc disorders with radiculopathy, lumbosacral region
- M51.A3 Intervertebral annulus fibrosus defect, lumbosacral region, unspecified size: , if applicable, lumbosacral disc herniation (M51.17, M51.27)
- M51.A4 Intervertebral annulus fibrosus defect, small, lumbosacral region: , if applicable, lumbosacral disc herniation (M51.17, M51.27)
- M51.A5 Intervertebral annulus fibrosus defect, large, lumbosacral region: , if applicable, lumbosacral disc herniation (M51.17, M51.27)
- M51.26 Other intervertebral disc displacement, lumbar region
- M51.A0 Intervertebral annulus fibrosus defect, lumbar region, unspecified size: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.A1 Intervertebral annulus fibrosus defect, small, lumbar region: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.A2 Intervertebral annulus fibrosus defect, large, lumbar region: , if applicable, lumbar disc herniation (M51.06, M51.16, M51.26)
- M51.27 Other intervertebral disc displacement, lumbosacral region
- M51.A3 Intervertebral annulus fibrosus defect, lumbosacral region, unspecified size: , if applicable, lumbosacral disc herniation (M51.17, M51.27)
- M51.A4 Intervertebral annulus fibrosus defect, small, lumbosacral region: , if applicable, lumbosacral disc herniation (M51.17, M51.27)
- M51.A5 Intervertebral annulus fibrosus defect, large, lumbosacral region: , if applicable, lumbosacral disc herniation (M51.17, M51.27)
- M89.7 Major osseous defect: osteoporosis (M80.-, M81.-)
- M89.7 Major osseous defect: osteoporosis (M80.-, M81.-)
- M89.7 Major osseous defect: osteomyelitis (M86.-)
- L62 Nail disorders in diseases classified elsewhere: pachydermoperiostosis (M89.4-)
- M89.7 Major osseous defect: osteolysis (M89.5-)
- M94.3 Chondrolysis: any associated slipped upper femoral epiphysis (nontraumatic) (M93.0-)
The first view lists notes printed in this chapter (a note on a category or block applies to every code beneath it). The second lists codes of this chapter named by Code First Notes anywhere in the Tabular List, including notes in other chapters.
Questions About Code First Notes
What does a Code First note mean?
A Code First note means the underlying condition named in the note is sequenced before the code that carries the note. Under the etiology/manifestation convention, a “code first” note appears at the manifestation code and a “use additional code” note at the etiology code (Section I.A.13). The FY 2027 Tabular List has 810 of them; 600 name other codes, with 736 references to 429 distinct codes, categories and ranges.
Can a code with a Code First note be the principal diagnosis?
Not when it is a manifestation code. Codes titled “in diseases classified elsewhere” are never permitted as the first-listed or principal diagnosis; they must follow the underlying condition. The etiology and manifestation page lists them all.
Related References
Source: FY 2027 ICD-10-CM Tabular List (CMS and NCHS) and the ICD-10-CM Official Guidelines for Coding and Reporting FY 2027, Section I.A. ICD List is not affiliated with CMS or NCHS.