M89.8
Non-billableOther specified disorders of bone
Other specified disorders of bone
This is a header/category code. For billing purposes, use a more specific child code from the list below.
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Infantile cortical hyperostoses
- Post-traumatic subperiosteal ossification
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
Child Codes (1)
Related Codes(9)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(55)
UMLS
- CAFFEY DISEASEC0020497
- CAFYDC0020497
- CONGEN HYPEROSTOSIS CORTICALC0020497
- CORTICAL CONGEN HYPEROSTOSISC0020497
- CORTICAL HYPEROSTOSIS CONGENC0020497
- Caffey De Toni Silvermann SyndromeC0020497
- Caffey DiseaseC0020497
- Caffey diseaseC0020497
- Caffey syndromeC0020497
- Caffey's Disease, FamilialC0020497
- Caffey's diseaseC0020497
- Caffey-De Toni-Silvermann SyndromeC0020497
- Caffey-Silverman syndromeC0020497
- Congenital Cortical HyperostosesC0020497
- Congenital Cortical HyperostosisC0020497
- Congenital Hyperostoses, CorticalC0020497
- Congenital Hyperostosis, CorticalC0020497
- Cortical Congenital HyperostosesC0020497
- Cortical Congenital HyperostosisC0020497
- Cortical Hyperostoses, CongenitalC0020497
- Cortical Hyperostoses, InfantileC0020497
- Cortical Hyperostosis, CongenitalC0020497
- Cortical Hyperostosis, InfantileC0020497
- De Toni-Caffey diseaseC0020497
- Disease, CaffeyC0020497
- Disease, Familial Caffey'sC0020497
- Familial Caffey DiseaseC0020497
- Familial Caffey's DiseaseC0020497
- Familial Caffeys DiseaseC0020497
- Familial Infantile Cortical HyperostosisC0020497
- Familial infantile cortical hyperostosisC0020497
- HYPEROSTOSIS CORTICAL CONGENC0020497
- Hyperostoses, Congenital CorticalC0020497
- Hyperostoses, Cortical CongenitalC0020497
- Hyperostoses, Infantile CorticalC0020497
- Hyperostosis, Congenital CorticalC0020497
- Hyperostosis, Cortical CongenitalC0020497
- Hyperostosis, Cortical, CongenitalC0020497
- Hyperostosis, Infantile CorticalC0020497
- INFANTILE CORTICAL HYPEROSTOSISC0020497
- Infantile Cortical HyperostosesC0020497
- Infantile Cortical HyperostosisC0020497
- Infantile cortical hyperostosesC0020497
- Infantile cortical hyperostosisC0020497
- Infantile cortical hyperostosis (disorder)C0020497
- Syndrome, Caffey-De Toni-SilvermannC0020497
- caffey diseaseC0020497
- caffey syndromeC0020497
- caffey's diseaseC0020497
- infantile cortical hyperostosisC0020497
- Ossification of subperiosteum due to and following traumatic injuryC2902419
- Ossification of subperiosteum due to and following traumatic injury (disorder)C2902419
- Post-traumatic subperiosteal ossificationC2902419
- Other specified disorders of boneC0477691
- Other specified disorders of bone, unspecified siteC0477691
Frequently Asked Questions
What is the ICD-10 code for other specified disorders of bone?
The ICD-10-CM code for other specified disorders of bone is M89.8. The full clinical description is "Other specified disorders of bone". M89.8 is a non-billable header code. Use a more specific child code for billing purposes.
What does ICD-10 code M89.8 mean?
ICD-10-CM code M89.8 represents “Other specified disorders of bone”. It is classified under Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue and is a non-billable header code. Use a more specific child code for billing purposes.
Is M89.8 a billable code?
No, M89.8 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 1 child codes under M89.8.
What chapter is M89.8 in?
M89.8 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M89.8?
M89.8 has Excludes1 notes indicating codes that cannot be used together with it, including: postprocedural osteopathies (M96.-).
What are the subcategories under M89.8?
M89.8 has 1 child code, including: M89.8X (Other specified disorders of bone).
What are the UMLS CUIs for M89.8?
M89.8 is linked to 3 UMLS Concept Unique Identifiers: C0020497, C2902419, C0477691. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does M89.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified disorders of bone 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 M89.8?
M89.8 maps to the ICD-11 code: FB86.Z (Disorders associated with bone growth, unspecified).
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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.