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211 Sickle-cell/Hb-C disease with acute chest syndrome
- D57.212 Sickle-cell/Hb-C disease with splenic sequestration
- D57.219 Sickle-cell/Hb-C disease with crisis, unspecified
- Sickle-cell/Hb-C disease with crisis NOS
- D57.3 Sickle-cell trait
- Hb-S trait
- Heterozygous hemoglobin S
- D57.4 Sickle-cell thalassemia
- Sickle-cell beta thalassemia
- Thalassemia Hb-S disease
- D57.40 Sickle-cell thalassemia without crisis
- Sickle-cell thalassemia NOS
- D57.41 Sickle-cell thalassemia with crisis
- Sickle-cell thalassemia with vasoocclusive pain
- D57.411 Sickle-cell thalassemia with acute chest syndrome
- D57.412 Sickle-cell thalassemia with splenic sequestration
- D57.419 Sickle-cell thalassemia with crisis, unspecified
- Sickle-cell thalassemia with crisis NOS
- D57.8 Other sickle-cell disorders
- Hb-SD disease
- Hb-SE disease
- D57.80 Other sickle-cell disorders without crisis
- D57.81 Other sickle-cell disorders with crisis
- D57.811 Other sickle-cell disorders with acute chest syndrome
- D57.812 Other sickle-cell disorders with splenic sequestration
- D57.819 Other sickle-cell disorders with crisis, unspecified
- Other sickle-cell disorders with crisis NOS
D58 Other hereditary hemolytic anemias
- Excludes1: hemolytic anemia of the newborn (P55.-)
- D58.0 Hereditary spherocytosis
- Acholuric (familial) jaundice
- Congenital (spherocytic) hemolytic icterus
- Minkowski-Chauffard syndrome
- D58.1 Hereditary elliptocytosis
- Elliptocytosis (congenital)
- Ovalocytosis (congenital) (hereditary)
- D58.2 Other hemoglobinopathies
- Abnormal hemoglobin NOS
- Congenital Heinz body anemia
- Hb-C disease
- Hb-
