M34.9
BillableSystemic sclerosis, unspecified
Systemic sclerosis, unspecified
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)
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)
Also Known As / Clinical Terms
SNOMED CT
- Biliary cirrhosis1761006
- Cholangitic cirrhosis1761006
- Cholestatic cirrhosis1761006
- Chronic nonsuppurative destructive cholangitis1761006
- Thickening of skin17417006
- Hanot's cirrhosis31712002
- Primary biliary cholangitis31712002
- Primary biliary cirrhosis31712002
- Dilated cardiomyopathy due to systemic sclerosis35719004
- Biliary duct fibrosis48124008
- Biliary sclerosis48124008
- Fibrosis of bile duct48124008
- Hypothyroidism due to scleroderma63115005
- Pericarditis co-occurrent and due to scleroderma87442008
- Pericarditis due to systemic sclerosis87442008
- Pericarditis secondary to scleroderma87442008
- SS - Systemic sclerosis89155008
- Systemic scleroderma89155008
- Systemic sclerosis89155008
- Thibierge-Weissenbach syndrome89155008
- Buschke's scleredema95323007
- Scleredema95323007
- Scleredema adultorum of Buschke95323007
- Induration of subcutaneous fat95350002
- Sclerema95350002
- Diffuse cutaneous scleroderma128460000
- Diffuse cutaneous systemic sclerosis128460000
- Diffuse scleroderma128460000
- Diffuse systemic sclerosis128460000
- Systemic sclerosis, diffuse128460000
- Autoimmune liver disease235890007
- Renal involvement in scleroderma236502006
- Scleroderma267874003
- Acrosclerosis298285004
- Limited cutaneous systemic sclerosis298285004
- Systemic sclerosis with limited cutaneous involvement298285004
- Limited scleroderma299276009
- Limited systemic sclerosis299276009
- Systemic sclerosis, limited299276009
- Cholangiohepatitis370489002
- Hypermelanosis due to connective tissue disorder402614008
- Necrotising vasculitis secondary to connective tissue disease402657003
- Necrotizing vasculitis secondary to connective tissue disease402657003
- Occupational scleroderma402712002
- Cutaneous complication of systemic sclerosis402713007
- Telangiectasia of nailfolds402834007
- Calcinosis cutis due to systemic sclerosis403514006
- Scleroderma-associated calcinosis403514006
- Hypermelanosis due to systemic sclerosis403515007
- Scleroderma-associated hypermelanosis403515007
- Scleroderma-associated telangiectasia403516008
- Telangiectasia due to systemic sclerosis403516008
- Scleroderma-associated nailfold telangiectasia403517004
- Telangiectasia of nailfolds due to systemic sclerosis403517004
- Necrotising vasculitis due to scleroderma403518009
- Necrotizing vasculitis due to scleroderma403518009
- Scleroderma-associated necrotising vasculitis403518009
- Scleroderma-associated necrotizing vasculitis403518009
- Poikiloderma due to scleroderma403519001
- Poikiloscleroderma403519001
- Scleroderma-associated poikiloderma403519001
- Nail dystrophy due to systemic sclerosis403520007
- Scleroderma-associated nail dystrophy403520007
- Autoimmune hepatitis408335007
- PSS - Progressive systemic sclerosis444133002
- Progressive systemic sclerosis444133002
- Autoimmune cholangitis713654004
- Primary biliary cirrhosis co-occurrent with systemic scleroderma715401008
- Reynolds syndrome715401008
- Paediatric onset systemic sclerosis724603009
- Pediatric onset systemic sclerosis724603009
- Cardiomyopathy due to connective tissue disease860837007
- Gingival disease due to scleroderma1197016009
- Gingival disease due to systemic sclerosis1197016009
- Post-infectious scleredema1258980000
- Post-infectious scleroedema1258980000
- Scleredema due to and following infectious disease1258980000
- Scleroedema due to and following infectious disease1258980000
- Hypothyroidism due to systemic sclerosis1264402008
- Dilated cardiomyopathy due to scleroderma1264404009
- Glomerulonephritis co-occurrent and due to scleroderma89681000119101
UMLS
- Diffuse SclerodermaC0036421
- Diffuse SclerosisC0036421
- PSS (progressive systemic sclerosis)C0036421
- Progressive Systemic SclerosisC0036421
- Progressive systemic sclerosisC0036421
- SS - Systemic sclerosisC0036421
- Scleroderma, DiffuseC0036421
- Scleroderma, SystemicC0036421
- Sclerosis, SystemicC0036421
- Systemic SclerodermaC0036421
- Systemic SclerosisC0036421
- Systemic sclerodermaC0036421
- Systemic sclerosisC0036421
- Systemic sclerosis (disorder)C0036421
- Systemic sclerosis, unspecifiedC0036421
- progressive systemic sclerosisC0036421
- sclerodermaC0036421
- sclerodermasC0036421
- systemic sclerodermaC0036421
- systemic sclerosisC0036421
Frequently Asked Questions
What is the ICD-10 code for systemic sclerosis, unspecified?
The ICD-10-CM code for systemic sclerosis, unspecified is M34.9. The full clinical description is "Systemic sclerosis, unspecified". M34.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M34.9 mean?
ICD-10-CM code M34.9 represents "Systemic sclerosis, unspecified". 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 M34.9 a billable code?
Yes, M34.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M34.9 in?
M34.9 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M34.9?
M34.9 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 M34.9 map to?
M34.9 maps to 40 SNOMED CT concepts: 298285004, 713654004, 408335007, 235890007, 1761006, and 35 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M34.9?
M34.9 is linked to 1 UMLS Concept Unique Identifier: C0036421. 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.