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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-