D75.0

Familial erythrocytosis

Billable code

This code does not map to a risk-adjusting HCC in the loaded models.

Coding notes

Excludes 1 never coded together · Excludes 2 may co-exist

This code · D75.0

Excludes 1

hereditary ovalocytosis (D58.1)

Synonyms

Benign polycythemia Familial polycythemia

Inherited from D75Other and unsp diseases of blood and blood-forming organs

Excludes 2

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)

Inherited from chapter 3Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Excludes 2

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)

Official Guidelines for D75.0

FY 2026 ›

I.C.3Chapter-specific guidanceChapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)

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