D75.81
BillableMyelofibrosis
Myelofibrosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Myelofibrosis NOS
- Secondary myelofibrosis NOS
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
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •acute lymphadenitisL04
- •chronic lymphadenitisI88.1
- •enlarged lymph nodesR59
- •hypergammaglobulinemia NOSD89.2
- •lymphadenitis NOSI88.9
- •mesenteric lymphadenitis (acute) (chronic)I88.0
Code First
The underlying condition must be sequenced before this code
- the underlying disorder, such as:
- •malignant neoplasm of breastC50
Use Additional Code
Additional codes that should follow this code
Related Codes(4)
Also Known As / Clinical Terms(82)
SNOMED CT
- Agnogenic myeloid metaplasia52967002
- MF - Myelofibrosis52967002
- Myelofibrosis52967002
- Myelosclerosis52967002
- Ischaemic myelofibrosis699293000
- Ischemic myelofibrosis699293000
- Congenital neutropenia, bone marrow fibrosis, nephromegaly syndrome775909002
- Congenital neutropenia, myelofibrosis, nephromegaly syndrome775909002
- VPS45 deficiency775909002
- Myelofibrosis due to and following polycythaemia vera871540009
- Myelofibrosis due to and following polycythemia vera871540009
- Post-polycythaemia vera myelofibrosis871540009
- Post-polycythemia vera myelofibrosis871540009
- Myelofibrosis due to and following essential thrombocythaemia871541008
- Myelofibrosis due to and following essential thrombocythemia871541008
- Post-essential thrombocythaemia myelofibrosis871541008
- Post-essential thrombocythemia myelofibrosis871541008
- Drug induced myelofibrosis1153374001
- Myelofibrosis caused by drug1153374001
- Hereditary thrombocytopenia with early-onset myelofibrosis1172699002
- Myelofibrosis due to another disorder119031000119101
- Secondary myelofibrosis119031000119101
UMLS
- Agnogenic myeloid metaplasiaC0026987
- MF - MyelofibrosisC0026987
- MMMC0026987
- MYELOFIBROSISC0026987
- MYELOFIBROSIS WITH MYELOID METAPLASIAC0026987
- MyelofibrosisC0026987
- Myelofibrosis (disorder)C0026987
- Myelofibrosis NOSC0026987
- Myelofibrosis with myeloid metaplasiaC0026987
- MyelosclerosisC0026987
- Myelosis non-leukaemicC0026987
- Myelosis non-leukemicC0026987
- Myelosis-non-leukaemicC0026987
- bone fibrosis marrowC0026987
- bone marrow fibrosisC0026987
- chronic idiopathic myelofibrosisC0026987
- fibrosis bone marrowC0026987
- mosC0026987
- myelofibrosisC0026987
- myelosclerosisC0026987
- Myelofibrosis due to another disorderC0242006
- Myelofibrosis due to another disorder (disorder)C0242006
- Secondary MyelofibrosisC0242006
- Secondary myelofibrosisC0242006
- Secondary myelofibrosis NOSC0242006
Clinical Terms
- Myelofibrosis due to another disorder
- mos
- Myelosis-non-leukaemic
- MF - Myelofibrosis
- fibrosis bone marrow
- Drug induced myelofibrosis
- Myelosis non-leukaemic
- chronic idiopathic myelofibrosis
- Myelofibrosis with myeloid metaplasia
- Hereditary thrombocytopenia with early-onset myelofibrosis
- Myelosclerosis
- VPS45 deficiency
- Secondary myelofibrosis NOS
- Myelosis non-leukemic
- Secondary myelofibrosis
- Myelofibrosis due to and following essential thrombocythemia
- Myelofibrosis due to another disorder (disorder)
- Congenital neutropenia, myelofibrosis, nephromegaly syndrome
- Agnogenic myeloid metaplasia
- Myelofibrosis (disorder)
- Myelofibrosis NOS
- Myelofibrosis due to and following polycythaemia vera
- Ischaemic myelofibrosis
- Post-polycythemia vera myelofibrosis
- MMM
- Myelofibrosis due to and following polycythemia vera
- bone marrow fibrosis
- Post-polycythaemia vera myelofibrosis
- Congenital neutropenia, bone marrow fibrosis, nephromegaly syndrome
- Post-essential thrombocythaemia myelofibrosis
- bone fibrosis marrow
- Myelofibrosis due to and following essential thrombocythaemia
- Myelofibrosis caused by drug
- Post-essential thrombocythemia myelofibrosis
- Ischemic myelofibrosis
Frequently Asked Questions
What is the ICD-10 code for myelofibrosis?
The ICD-10-CM code for myelofibrosis is D75.81. The full clinical description is "Myelofibrosis". D75.81 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D75.81 mean?
ICD-10-CM code D75.81 represents “Myelofibrosis”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D75.81 a billable code?
Yes, D75.81 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D75.81 in?
D75.81 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D75.81?
D75.81 has Excludes1 notes indicating codes that cannot be used together with it, including: acute myelofibrosis (C94.4-); idiopathic myelofibrosis (D47.1); leukoerythroblastic anemia (D61.82); and 4 more.
Are additional codes required with D75.81?
Yes, when using D75.81, also report: code, if applicable, for associated therapy-related myelodysplastic syndrome (D46.-).
What SNOMED CT codes does D75.81 map to?
D75.81 maps to 8 SNOMED CT concepts: 52967002, 775909002, 1153374001, 1172699002, 699293000, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D75.81?
D75.81 is linked to 2 UMLS Concept Unique Identifiers: C0026987, C0242006. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D75.81 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like myelofibrosis 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 D75.81?
There is no direct ICD-11 mapping available for D75.81 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.