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D disease
- Hb-E disease
- Hemoglobinopathy NOS
- Unstable hemoglobin hemolytic disease
- Excludes1: familial polycythemia (D75.0)
- Hb-M disease (D74.0)
- hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
- high-altitude polycythemia (D75.1)
- methemoglobinemia (D74.-)
- D58.8 Other specified hereditary hemolytic anemias
- D58.9 Hereditary hemolytic anemia, unspecified
D59 Acquired hemolytic anemia
- D59.0 Drug-induced autoimmune hemolytic anemia
- Code first (T36-T50) to identify drug
- D59.1 Other autoimmune hemolytic anemias
- Autoimmune hemolytic disease (cold type) (warm type)
- Chronic cold hemagglutinin disease
- Cold agglutinin disease
- Cold agglutinin hemoglobinuria
- Cold type (secondary) (symptomatic) hemolytic anemia
- Warm type (secondary) (symptomatic) hemolytic anemia
- Excludes1: Evans syndrome (D69.41)
- hemolytic disease of newborn (P55.-)
- paroxysmal cold hemoglobinuria (D59.6)
- D59.2 Drug-induced nonautoimmune hemolytic anemia
- Drug-induced enzyme deficiency anemia
- Code first (T36-T50) to identify drug
- D59.3 Hemolytic-uremic syndrome
- D59.4 Other nonautoimmune hemolytic anemias
- Mechanical hemolytic anemia
- Microangiopathic hemolytic anemia
- Toxic hemolytic anemia
- D59.5 Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
- Excludes1: hemoglobinuria NOS (R82.3)
- D59.6 Hemoglobinuria due to hemolysis from other external causes
- Hemoglobinuria from exertion
- March hemoglobinuria
- Paroxysmal cold hemoglobinuria
- Use additional code (Chapter 20) to identify external cause
- Excludes1: hemoglobinuria NOS (R82.3)
- D59.8 Other acquired hemolytic anemias
- D59.9 Acquired hemolytic anemia, unspecified
- Idiopathic hemolytic anemia, chronic
=Aplastic
