M61.10
BillableMyositis ossificans progressiva, unspecified site
Myositis ossificans progressiva, unspecified site
Coding Notes
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 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
- •muscular dystrophies and myopathiesG71-G72
Related Codes(9)
M61.11Myositis ossificans progressiva, shoulder
M61.12Myositis ossificans progressiva, upper arm
M61.13Myositis ossificans progressiva, forearm
M61.14Myositis ossificans progressiva, hand and finger(s)
M61.15Myositis ossificans progressiva, thigh
M61.16Myositis ossificans progressiva, lower leg
M61.17Myositis ossificans progressiva, ankle, foot and toe(s)
M61.18Myositis ossificans progressiva, other site
M61.19Myositis ossificans progressiva, multiple sites
Also Known As / Clinical Terms(52)
SNOMED CT
- Myositis ossificans associated with dermato / polymyositis3458000
- Polymyositis ossificans3458000
- Disorder: ectopic bone tissue, congenital26155004
- Ectopic bone tissue, congenital26155004
- Postoperative heterotopic calcification80116000
- Diffuse progressive ossifying polymyositis82725007
- FOP - Fibrodysplasia ossificans progressiva82725007
- Fibrodysplasia ossificans congenita82725007
- Fibrodysplasia ossificans progressiva82725007
- Myositis ossificans progressiva82725007
- Münchmeyer disease82725007
- Progressive myositis ossificans82725007
- Postoperative heterotopic ossification444748003
UMLS
- Diffuse progressive ossifying polymyositisC0016037
- FIBRODYSPLASIA OSSIFICANS PROGRESSIVAC0016037
- FOPC0016037
- FOP - Fibrodysplasia ossificans progressivaC0016037
- Fibrodysplasia Ossificans ProgressivaC0016037
- Fibrodysplasia ossificans congenitaC0016037
- Fibrodysplasia ossificans progressivaC0016037
- Myositis Ossificans ProgressivaC0016037
- Myositis ossificans progressivaC0016037
- Myositis ossificans progressiva, unspecified siteC0016037
- Münchmeyer diseaseC0016037
- Progressive Myositis OssificansC0016037
- Progressive Ossifying MyositisC0016037
- Progressive myositis ossificansC0016037
- Progressive myositis ossificans (disorder)C0016037
- Progressive ossifying myositisC0016037
- Stone man syndromeC0016037
- muenchmeyer syndromeC0016037
- myositis ossificans progressivaC0016037
- progressive myositis ossificansC0016037
- progressive ossifying myositisC0016037
Clinical Terms
- FOP - Fibrodysplasia ossificans progressiva
- muenchmeyer syndrome
- Postoperative heterotopic ossification
- Stone man syndrome
- Ectopic bone tissue, congenital
- Myositis ossificans progressiva
- Fibrodysplasia Ossificans Progressiva
- Münchmeyer disease
- Fibrodysplasia ossificans congenita
- Polymyositis ossificans
- progressive ossifying myositis
- Postoperative heterotopic calcification
- Disorder: ectopic bone tissue, congenital
- Progressive myositis ossificans (disorder)
- Myositis ossificans associated with dermato / polymyositis
- FOP
- Progressive myositis ossificans
- Diffuse progressive ossifying polymyositis
Frequently Asked Questions
What is the ICD-10 code for myositis ossificans progressiva, unspecified site?
The ICD-10-CM code for myositis ossificans progressiva, unspecified site is M61.10. The full clinical description is "Myositis ossificans progressiva, unspecified site". M61.10 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M61.10 mean?
ICD-10-CM code M61.10 represents “Myositis ossificans progressiva, unspecified site”. 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 M61.10 a billable code?
Yes, M61.10 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M61.10 in?
M61.10 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M61.10?
M61.10 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 4 more.
What SNOMED CT codes does M61.10 map to?
M61.10 maps to 5 SNOMED CT concepts: 82725007, 26155004, 3458000, 80116000, 444748003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M61.10?
M61.10 is linked to 1 UMLS Concept Unique Identifier: C0016037. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does M61.10 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like myositis ossificans progressiva, unspecified site 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 M61.10?
There is no direct ICD-11 mapping available for M61.10 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.