D75.0
BillableFamilial erythrocytosis
Familial erythrocytosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Benign polycythemia
- Familial polycythemia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- hereditary ovalocytosis (D58.1)
Excludes 2
Conditions not included here, but the patient may have both
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- 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)
- acute lymphadenitis (L04.-)
- chronic lymphadenitis (I88.1)
- enlarged lymph nodes (R59.-)
- hypergammaglobulinemia NOS (D89.2)
- lymphadenitis NOS (I88.9)
- mesenteric lymphadenitis (acute) (chronic) (I88.0)
Also Known As / Clinical Terms
SNOMED CT
- Familial erythrocytosis17342003
- Familial polycythaemia17342003
- Familial polycythemia17342003
- Hereditary pure erythrocytosis17342003
- Disorder of manganese metabolism63656007
- Primary malignant neoplasm of bone marrow93720005
- Erythrocythaemia109992005
- Erythrocythemia109992005
- Osler-Vaquez syndrome109992005
- PPP - Primary proliferative polycythaemia109992005
- PPP - Primary proliferative polycythemia109992005
- PRV - Polycythaemia rubra vera109992005
- PRV - Polycythemia rubra vera109992005
- Polycythaemia rubra vera109992005
- Polycythaemia vera109992005
- Polycythaemia vera (clinical)109992005
- Polycythemia rubra vera109992005
- Polycythemia vera109992005
- Polycythemia vera (clinical)109992005
- Primary polycythaemia109992005
- Primary proliferative polycythaemia109992005
- Primary proliferative polycythemia109992005
- Vaquez's disease109992005
- Familial erythrocytosis due to diphosphoglycerate mutase deficiency127065001
- Familial polycythaemia vera127066000
- Familial polycythemia vera127066000
- HMDPC - hypermanganesemia with dystonia, polycythaemia and cirrhosis702377007
- HMDPC - hypermanganesemia with dystonia, polycythemia and cirrhosis702377007
- Hypermanganesemia with dystonia, polycythaemia, and cirrhosis702377007
- Hypermanganesemia with dystonia, polycythemia, and cirrhosis702377007
- Familial manganese-induced neurotoxicity768553002
- HMNDYT - hypermanganesemia with dystonia768553002
- Hypermanganesemia with dystonia768553002
- Chuvash erythrocytosis770407006
- Chuvash polycythaemia770407006
- Chuvash polycythemia770407006
- Von Hippel Lindau dependent polycythaemia770407006
- Von Hippel Lindau dependent polycythemia770407006
- Primary familial polycythaemia due to erythropoietin receptor mutation1153349004
- Primary familial polycythemia due to erythropoietin receptor mutation1153349004
UMLS
- Benign familial polycythemiaC0152264
- Congenital erythrocytosisC0152264
- Familial ErythrocytosisC0152264
- Familial PolycythemiaC0152264
- Familial erythrocytosisC0152264
- Familial erythrocytosis (disorder)C0152264
- Familial polycythaemiaC0152264
- Familial polycythemiaC0152264
- Hereditary erythrocytosisC0152264
- Hereditary pure erythrocytosisC0152264
- Primary familial polycythemiaC0152264
- Benign polycythaemiaC0221276
- Benign polycythemiaC0221276
- Relative erythrocytosisC0221276
- Relative polycythaemiaC0221276
- Relative polycythemiaC0221276
- Relative polycythemia (disorder)C0221276
- Spurious polycythaemiaC0221276
- Spurious polycythemiaC0221276
- polycythemia relativeC0221276
- pseudopolycythemiaC0221276
- relative erythrocytosisC0221276
- relative polycythemiaC0221276
- spurious polycythemiaC0221276
Frequently Asked Questions
What is ICD-10 code D75.0?
ICD-10-CM code D75.0 represents "Familial erythrocytosis". It is a billable/specific code that can be used on a claim.
Is D75.0 a billable code?
Yes, D75.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D75.0 in?
D75.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D75.0?
D75.0 has Excludes1 notes indicating codes that cannot be used together with it, including: hereditary ovalocytosis (D58.1).
What SNOMED CT codes does D75.0 map to?
D75.0 maps to 10 SNOMED CT concepts: 770407006, 63656007, 109992005, 17342003, 127065001, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D75.0?
D75.0 is linked to 2 UMLS Concept Unique Identifiers: C0152264, C0221276. 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.