D75.89
BillableOther specified diseases of blood and blood-forming organs
Other specified diseases of blood and blood-forming organs
Coding Notes
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
Related Codes(4)
Also Known As / Clinical Terms(247)
SNOMED CT
- Acquired pancytopenia5876000
- Pancytopenia - acquired5876000
- Anaemia caused by radiation9764001
- Anaemia due to radiation9764001
- Anemia caused by radiation9764001
- Anemia due to radiation9764001
- Bone marrow hyperplasia10138007
- Haematopoietic cell proliferation10138007
- Hematopoietic cell proliferation10138007
- Hyperviscosity syndrome11888009
- Reimann's syndrome11888009
- Bone marrow maturation arrest14998000
- Haematopoietic maturation arrest14998000
- Hematopoietic maturation arrest14998000
- Benign lymphoid hyperplasia19750001
- Pseudolymphoma19750001
- Neutrophilic hyperplasia of bone marrow20888002
- AL amyloidosis23132008
- Amyloid light-chain amyloidosis23132008
- Primary amyloidosis of light chain type23132008
- Acute vomiting23971007
- Congenital anomaly of the haematopoietic system40888008
- Congenital anomaly of the hematopoietic system40888008
- Complete trisomy 21 syndrome41040004
- Down syndrome41040004
- Downs syndrome41040004
- T21 - Trisomy 2141040004
- Extramedullary haematopoiesis42952007
- Extramedullary hematopoiesis42952007
- Cytopenia50820005
- Light chain disease51319002
- Eosinophilic hyperplasia of bone marrow57375005
- Hyperviscosity64088006
- Erythroid hyperplasia of bone marrow68164004
- Myeloid hyperplasia of bone marrow70918005
- Plasma cell hyperplasia of bone marrow70958007
- Megakaryocytic hyperplasia of bone marrow83525004
- Abnormal megakaryocyte production103211000
- Non-malignant lymphocyte AND/OR plasma cell disorder105603000
- Anaemia caused by physical agent111581008
- Anemia caused by physical agent111581008
- Granulocytic hyperplasia of bone marrow123616008
- Primary cytopenia123718001
- Mild cytopenia123720003
- Moderate cytopenia123721004
- Severe cytopenia123722006
- Toxic cytopenia123723001
- Transitory cytopenia123724007
- Mild bone marrow hyperplasia123725008
- Moderate bone marrow hyperplasia123726009
- Severe bone marrow hyperplasia123727000
- Recurrent bone marrow hyperplasia123728005
- Deficiency of hexokinase124297004
- Deficiency of hexokinase type IV124297004
- HK - Hexokinase deficiency124297004
- Hexokinase deficiency124297004
- Reticulocytopenia124961001
- Haemolytic disorder128086004
- Hemolytic disorder128086004
- Reticulocyte count abnormal165685003
- Reticulocyte count outside reference range165685003
- Non-anaemic red cell disorder234338001
- Non-anemic red cell disorder234338001
- Macrocytosis - no anaemia234339009
- Macrocytosis - no anemia234339009
- Alcohol-related macrocytosis234341005
- Deficiency of phosphotriose isomerase234405009
- Deficiency of triosephosphate mutase234405009
- TPI - Thiose phosphate isomerase deficiency234405009
- Triose phosphate isomerase deficiency234405009
- Blood group deletion syndrome234411007
- McLeod syndrome234411007
- T-cell mediated cytopenia276268001
- Alcoholic macrocytosis278363000
- Sideropenic anaemia with reticuloendothelial siderosis290246007
- Sideropenic anemia with reticuloendothelial siderosis290246007
- Bone marrow depression307762000
- Bone marrow failure307762000
- Finding of red blood cell size365622001
- Red blood cell size365622001
- Red blood cell size - finding365622001
- Blood viscosity level365651002
- Blood viscosity level - finding365651002
- Finding of blood viscosity level365651002
- Bone marrow myeloid cells365834007
- Bone marrow myeloid cells - finding365834007
- Finding of bone marrow myeloid cells365834007
- Finding of bone marrow erythropoiesis365835008
- Radiation sickness370402009
- Radiation-induced vomiting370402009
- Bone marrow suppression370569000
- Myelosuppression370569000
- Macrocytosis397073000
- Macrocytosis, red cells397073000
- Primary systemic amyloidosis associated with occult plasma cell dyscrasia402454000
- Primary systemic amyloidosis due to occult plasma cell dyscrasia402454000
- Blood viscosity above reference range414479006
- Increased blood viscosity414479006
- Ineffective haematopoiesis445961003
- Ineffective hematopoiesis445961003
- Ineffective hemopoiesis445961003
- Erythroid dysplasia of bone marrow703392003
- Transient abnormal myelopoiesis721307000
- H-ARS - Haematopoietic subsyndrome of acute radiation syndrome723489005
- H-ARS - Hematopoietic subsyndrome of acute radiation syndrome723489005
- Haematopoietic subsyndrome of acute radiation syndrome723489005
- Hematopoietic subsyndrome of acute radiation syndrome723489005
- Transient abnormal myelopoiesis and Down syndrome724643004
- Transient abnormal myelopoiesis co-occurrent with Down syndrome724643004
- OSLAM (osteosarcoma, limb anomalies, erythroid macrocytosis) syndrome733064004
- OSLAM syndrome733064004
- Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome733064004
- Dysplasia of megakaryocyte cell1142192003
- Megakaryocyte dysplasia1142192003
- Chemotherapy-induced myelosuppression1177084005
- Myelosuppression due to chemotherapy1177084005
- Polyclonal hyperviscosity syndrome1251448003
- Acute radiation sickness1260191006
- Acute radiation syndrome1260191006
- Disorder of bone marrow caused by ionising radiation1339017006
- Disorder of bone marrow caused by ionizing radiation1339017006
- Edema of bone marrow6411000179107
- Oedema of bone marrow6411000179107
Clinical Terms
- Haematopoietic subsyndrome of acute radiation syndrome
- Polyclonal hyperviscosity syndrome
- Myeloid hyperplasia of bone marrow
- Primary systemic amyloidosis associated with occult plasma cell dyscrasia
- Alcohol-related macrocytosis
- Primary amyloidosis of light chain type
- Ineffective hemopoiesis
- Blood viscosity level - finding
- Eosinophilic hyperplasia of bone marrow
- Hyperviscosity
- Macrocytosis - no anemia
- Radiation-induced vomiting
- Disorder of bone marrow caused by ionising radiation
- Mild cytopenia
- Macrocytosis - no anaemia
- OSLAM (osteosarcoma, limb anomalies, erythroid macrocytosis) syndrome
- Dysplasia of megakaryocyte cell
- Blood viscosity above reference range
- Granulocytic hyperplasia of bone marrow
- Erythroid dysplasia of bone marrow
- Primary cytopenia
- Haemolytic disorder
- TPI - Thiose phosphate isomerase deficiency
- Macrocytosis
- Myelosuppression
- Non-anaemic red cell disorder
- T21 - Trisomy 21
- Megakaryocyte dysplasia
- Benign lymphoid hyperplasia
- Abnormal megakaryocyte production
- McLeod syndrome
- Primary systemic amyloidosis due to occult plasma cell dyscrasia
- Finding of blood viscosity level
- Oedema of bone marrow
- Disorder of bone marrow caused by ionizing radiation
- Deficiency of hexokinase type IV
- Transient abnormal myelopoiesis and Down syndrome
- Haematopoietic maturation arrest
- Anaemia caused by radiation
- Increased blood viscosity
- Anaemia due to radiation
- Deficiency of hexokinase
- Edema of bone marrow
- Finding of bone marrow myeloid cells
- Deficiency of triosephosphate mutase
- Extramedullary hematopoiesis
- Pseudolymphoma
- Ineffective hematopoiesis
- Bone marrow failure
- Finding of bone marrow erythropoiesis
- OSLAM syndrome
- Radiation sickness
- Sideropenic anemia with reticuloendothelial siderosis
- H-ARS - Hematopoietic subsyndrome of acute radiation syndrome
- Acute radiation syndrome
- Acute radiation sickness
- Anaemia caused by physical agent
- Non-anemic red cell disorder
- Hematopoietic maturation arrest
- Red blood cell size - finding
- Moderate bone marrow hyperplasia
- Myelosuppression due to chemotherapy
- Transitory cytopenia
- Hexokinase deficiency
- HK - Hexokinase deficiency
- Bone marrow hyperplasia
- Finding of red blood cell size
- Severe bone marrow hyperplasia
- Mild bone marrow hyperplasia
- T-cell mediated cytopenia
- Complete trisomy 21 syndrome
- Bone marrow myeloid cells
- Hematopoietic cell proliferation
- Sideropenic anaemia with reticuloendothelial siderosis
- Plasma cell hyperplasia of bone marrow
- Ineffective haematopoiesis
- Bone marrow suppression
- Triose phosphate isomerase deficiency
- Anemia caused by physical agent
- Erythroid hyperplasia of bone marrow
- Hemolytic disorder
- Congenital anomaly of the haematopoietic system
- Acute vomiting
- Deficiency of phosphotriose isomerase
- Extramedullary haematopoiesis
- Down syndrome
- Acquired pancytopenia
- Bone marrow depression
- Downs syndrome
- Hematopoietic subsyndrome of acute radiation syndrome
- Transient abnormal myelopoiesis co-occurrent with Down syndrome
- Anemia caused by radiation
- Blood viscosity level
- Moderate cytopenia
- Haematopoietic cell proliferation
- Transient abnormal myelopoiesis
- Alcoholic macrocytosis
- Blood group deletion syndrome
- Reticulocyte count outside reference range
- Neutrophilic hyperplasia of bone marrow
- Reticulocytopenia
- Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome
- Macrocytosis, red cells
- H-ARS - Haematopoietic subsyndrome of acute radiation syndrome
- AL amyloidosis
- Toxic cytopenia
- Congenital anomaly of the hematopoietic system
- Cytopenia
- Hyperviscosity syndrome
- Anemia due to radiation
- Pancytopenia - acquired
- Severe cytopenia
- Reimann's syndrome
- Reticulocyte count abnormal
- Recurrent bone marrow hyperplasia
- Chemotherapy-induced myelosuppression
- Bone marrow maturation arrest
- Non-malignant lymphocyte AND/OR plasma cell disorder
- Red blood cell size
- Bone marrow myeloid cells - finding
- Light chain disease
- Megakaryocytic hyperplasia of bone marrow
- Amyloid light-chain amyloidosis
Frequently Asked Questions
What is the ICD-10 code for other specified diseases of blood and blood-forming organs?
The ICD-10-CM code for other specified diseases of blood and blood-forming organs is D75.89. The full clinical description is "Other specified diseases of blood and blood-forming organs". D75.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D75.89 mean?
ICD-10-CM code D75.89 represents “Other specified diseases of blood and blood-forming organs”. 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 D75.89 a billable code?
Yes, D75.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D75.89 in?
D75.89 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What SNOMED CT codes does D75.89 map to?
D75.89 maps to 68 SNOMED CT concepts: 23132008, 103211000, 5876000, 1260191006, 23971007, and 63 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D75.89?
D75.89 is linked to 1 UMLS Concept Unique Identifier: C0029768. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D75.89 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified diseases of blood and blood-forming organs 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 D75.89?
There is no direct ICD-11 mapping available for D75.89 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.