M34.89
BillableOther systemic sclerosis
Other systemic sclerosis
Coding Notes
Includes
Conditions included under this code
- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- autoimmune disease, single organ or single cell-type -code to relevant condition category
- •circumscribed sclerodermaL94.0
- •neonatal sclerodermaP83.88
Excludes 2
Conditions not included here, but the patient may have both
- •arthropathic psoriasisL40.5
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •compartment syndrome (traumatic)A-)T79
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(3)
Also Known As / Clinical Terms(76)
SNOMED CT
- Thickening of skin17417006
- Buschke's scleredema95323007
- Scleredema95323007
- Scleredema adultorum of Buschke95323007
- Diffuse cutaneous scleroderma128460000
- Diffuse cutaneous systemic sclerosis128460000
- Diffuse scleroderma128460000
- Diffuse systemic sclerosis128460000
- Systemic sclerosis, diffuse128460000
- Systemic sclerosis sine scleroderma128461001
- Systemic sclerosis without skin thickening128461001
- Renal involvement in scleroderma236502006
- Acute scleroderma renal crisis236503001
- Acrosclerosis298285004
- Limited cutaneous systemic sclerosis298285004
- Systemic sclerosis with limited cutaneous involvement298285004
- Limited scleroderma299276009
- Limited systemic sclerosis299276009
- Systemic sclerosis, limited299276009
- Chronic graft versus host disease402356004
- Chronic graft-versus-host disease402356004
- Sclerodermoid chronic graft-versus-host disease402358003
- Porphyria-induced scleroderma402481000
- Scleroderma due to porphyria402481000
- Cutaneous graft-versus-host disease444547006
- Graft versus host disease of skin444547006
- Paediatric onset systemic sclerosis724603009
- Pediatric onset systemic sclerosis724603009
- Diffuse paediatric systemic sclerosis1144925008
- Diffuse pediatric systemic sclerosis1144925008
- Diffuse systemic sclerosis of childhood1144925008
- Paraproteinaemia-associated scleroedema1254862001
- Paraproteinemia-associated scleredema1254862001
- Scleredema associated with monoclonal gammopathy1254862001
- Scleredema associated with paraproteinemia1254862001
- Scleroedema associated with monoclonal gammopathy1254862001
- Scleroedema associated with paraproteinaemia1254862001
Clinical Terms
- Porphyria-induced scleroderma
- Systemic sclerosis sine scleroderma
- Diffuse scleroderma
- Buschke's scleredema
- Scleroedema associated with monoclonal gammopathy
- Pediatric onset systemic sclerosis
- Systemic sclerosis, diffuse
- Scleredema adultorum of Buschke
- Systemic sclerosis with limited cutaneous involvement
- Diffuse systemic sclerosis of childhood
- Scleredema associated with monoclonal gammopathy
- Limited cutaneous systemic sclerosis
- Paraproteinaemia-associated scleroedema
- Sclerodermoid chronic graft-versus-host disease
- Thickening of skin
- Limited systemic sclerosis
- Scleroedema associated with paraproteinaemia
- Scleredema associated with paraproteinemia
- Diffuse cutaneous scleroderma
- Acute scleroderma renal crisis
- Systemic sclerosis, limited
- Diffuse pediatric systemic sclerosis
- Systemic sclerosis without skin thickening
- Diffuse cutaneous systemic sclerosis
- Paediatric onset systemic sclerosis
- Acrosclerosis
- Graft versus host disease of skin
- Diffuse paediatric systemic sclerosis
- Limited scleroderma
- Chronic graft-versus-host disease
- Scleredema
- Paraproteinemia-associated scleredema
- Cutaneous graft-versus-host disease
- Diffuse systemic sclerosis
- Chronic graft versus host disease
- Scleroderma due to porphyria
- Renal involvement in scleroderma
Frequently Asked Questions
What is the ICD-10 code for other systemic sclerosis?
The ICD-10-CM code for other systemic sclerosis is M34.89. The full clinical description is "Other systemic sclerosis". M34.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M34.89 mean?
ICD-10-CM code M34.89 represents “Other systemic sclerosis”. 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 M34.89 a billable code?
Yes, M34.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M34.89 in?
M34.89 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M34.89?
M34.89 has Excludes1 notes indicating codes that cannot be used together with it, including: autoimmune disease, single organ or single cell-type -code to relevant condition category; circumscribed scleroderma (L94.0); neonatal scleroderma (P83.88).
What SNOMED CT codes does M34.89 map to?
M34.89 maps to 15 SNOMED CT concepts: 298285004, 236503001, 95323007, 402356004, 444547006, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M34.89?
M34.89 is linked to 1 UMLS Concept Unique Identifier: C2895198. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does M34.89 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other systemic sclerosis 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 M34.89?
There is no direct ICD-11 mapping available for M34.89 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.