Hemolytic anemias (D55-D59)
D55Anemia due to enzyme disorders
Excludes 1: drug-induced enzyme deficiency anemia (D59.2)
D55.0Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
Favism
G6PD deficiency anemia
Excludes 1: glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia (D75.A)
D55.1Anemia due to other disorders of glutathione metabolism
Anemia (due to) enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway
Anemia (due to) hemolytic nonspherocytic (hereditary), type I
D55.2Anemia due to disorders of glycolytic enzymes
Excludes 1: disorders of glycolysis not associated with anemia (E74.81-)
D55.21Anemia due to pyruvate kinase deficiency
PK deficiency anemia
Pyruvate kinase deficiency anemia
D55.29Anemia due to other disorders of glycolytic enzymes
Hexokinase deficiency anemia
Triose-phosphate isomerase deficiency anemia
D55.3Anemia due to disorders of nucleotide metabolism
D55.8Other anemias due to enzyme disorders
D55.9Anemia due to enzyme disorder, unspecified
D56Thalassemia
Excludes 1: sickle-cell thalassemia (D57.4-)
D56.0Alpha thalassemia
Alpha thalassemia major
Hemoglobin H Constant Spring
Hemoglobin H disease
Hydrops fetalis due to alpha thalassemia
Severe alpha thalassemia
Triple gene defect alpha thalassemia
Use Additional Code: code, if applicable, for hydrops fetalis due to alpha thalassemia (P56.99)
Excludes 1: alpha thalassemia trait or minor (D56.3)
asymptomatic alpha thalassemia (D56.3)
hydrops fetalis due to isoimmunization (P56.0)
hydrops fetalis not due to immune hemolysis (P83.2)
D56.1Beta thalassemia
Beta thalassemia major
Cooley's anemia
Homozygous beta thalassemia
Severe beta thalassemia
Thalassemia intermedia
Thalassemia major
Excludes 1: beta thalassemia minor (D56.3)
beta thalassemia trait (D56.3)
delta-beta thalassemia (D56.2)
hemoglobin E-beta thalassemia (D56.5)
sickle-cell beta thalassemia (D57.4-)
D56.2Delta-beta thalassemia
Homozygous delta-beta thalassemia
Excludes 1: delta-beta thalassemia minor (D56.3)
delta-beta thalassemia trait (D56.3)
D56.3Thalassemia minor
Alpha thalassemia minor
Alpha thalassemia silent carrier
Alpha thalassemia trait
Beta thalassemia minor
Beta thalassemia trait
Delta-beta thalassemia minor
Delta-beta thalassemia trait
Thalassemia trait NOS
Excludes 1: alpha thalassemia (D56.0)
beta thalassemia (D56.1)
delta-beta thalassemia (D56.2)
hemoglobin E-beta thalassemia (D56.5)
sickle-cell trait (D57.3)
D56.4Hereditary persistence of fetal hemoglobin [HPFH]
D56.5Hemoglobin E-beta thalassemia
Excludes 1: beta thalassemia (D56.1)
beta thalassemia minor (D56.3)
beta thalassemia trait (D56.3)
delta-beta thalassemia (D56.2)
delta-beta thalassemia trait (D56.3)
hemoglobin E disease (D58.2)
other hemoglobinopathies (D58.2)
sickle-cell beta thalassemia (D57.4-)
D56.8Other thalassemias
Dominant thalassemia
Hemoglobin C thalassemia
Mixed thalassemia
Thalassemia with other hemoglobinopathy
Excludes 1: hemoglobin C disease (D58.2)
hemoglobin E disease (D58.2)
other hemoglobinopathies (D58.2)
sickle-cell anemia (D57.-)
sickle-cell thalassemia (D57.4-)
D56.9Thalassemia, unspecified
Mediterranean anemia (with other hemoglobinopathy)
D57Sickle-cell disorders
Use Additional Code: code for any associated fever (R50.81)
Excludes 1: other hemoglobinopathies (D58.-)
D57.0Hb-SS disease with crisis
Sickle-cell disease with crisis
Hb-SS disease with (vaso-occlusive) pain
D57.00Hb-SS disease with crisis, unspecified
Hb-SS disease with (painful) crisis NOS
Hb-SS disease with (vaso-occlusive) pain NOS
D57.01Hb-SS disease with acute chest syndrome
D57.02Hb-SS disease with splenic sequestration
D57.03Hb-SS disease with cerebral vascular involvement
Code Also: , if applicable, cerebral infarction (I63.-)
D57.04Hb-SS disease with dactylitis
D57.09Hb-SS disease with crisis with other specified complication
Use Additional Code: code to identify complications, such as:
cholelithiasis (K80.-)
priapism (N48.32)
D57.1Sickle-cell disease without crisis
Hb-SS disease without crisis
Sickle-cell anemia NOS
Sickle-cell disease NOS
Sickle-cell disorder NOS
D57.2Sickle-cell/Hb-C disease
Hb-SC disease
Hb-S/Hb-C disease
D57.20Sickle-cell/Hb-C disease without crisis
D57.21Sickle-cell/Hb-C disease with crisis
D57.211Sickle-cell/Hb-C disease with acute chest syndrome
D57.212Sickle-cell/Hb-C disease with splenic sequestration
D57.213Sickle-cell/Hb-C disease with cerebral vascular involvement
Code Also: , if applicable, cerebral infarction (I63.-)
D57.214Sickle-cell/Hb-C disease with dactylitis
D57.218Sickle-cell/Hb-C disease with crisis with other specified complication
Use Additional Code: code to identify complications, such as:
cholelithiasis (K80.-)
priapism (N48.32)
D57.219Sickle-cell/Hb-C disease with crisis, unspecified
Sickle-cell/Hb-C disease with crisis NOS
Sickle-cell/Hb-C disease with (vaso-occlusive) pain NOS
D57.3Sickle-cell trait
Hb-S trait
Heterozygous hemoglobin S
D57.4Sickle-cell thalassemia
Sickle-cell beta thalassemia
Thalassemia Hb-S disease
D57.40Sickle-cell thalassemia without crisis
Microdrepanocytosis
Sickle-cell thalassemia NOS
D57.41Sickle-cell thalassemia, unspecified, with crisis
Sickle-cell thalassemia with (painful) crisis NOS
Sickle-cell thalassemia with (vaso-occlusive) pain NOS
D57.411Sickle-cell thalassemia, unspecified, with acute chest syndrome
D57.412Sickle-cell thalassemia, unspecified, with splenic sequestration
D57.413Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
Code Also: , if applicable cerebral infarction (I63.-)
D57.414Sickle-cell thalassemia, unspecified, with dactylitis
D57.418Sickle-cell thalassemia, unspecified, with crisis with other specified complication
Use Additional Code: code to identify complications, such as:
cholelithiasis (K80.-)
priapism (N48.32)
D57.419Sickle-cell thalassemia, unspecified, with crisis
Sickle-cell thalassemia with (painful) crisis NOS
Sickle-cell thalassemia with (vaso-occlusive) pain NOS
D57.42Sickle-cell thalassemia beta zero without crisis
HbS-beta zero without crisis
Sickle-cell beta zero without crisis
D57.43Sickle-cell thalassemia beta zero with crisis
HbS-beta zero with crisis
Sickle-cell beta zero with crisis
D57.431Sickle-cell thalassemia beta zero with acute chest syndrome
HbS-beta zero with acute chest syndrome
Sickle-cell beta zero with acute chest syndrome
D57.432Sickle-cell thalassemia beta zero with splenic sequestration
HbS-beta zero with splenic sequestration
Sickle-cell beta zero with splenic sequestration
D57.433Sickle-cell thalassemia beta zero with cerebral vascular involvement
HbS-beta zero with cerebral vascular involvement
Sickle-cell beta zero with cerebral vascular involvement
Code Also: , if applicable cerebral infarction (I63.-)
D57.434Sickle-cell thalassemia beta zero with dactylitis
D57.438Sickle-cell thalassemia beta zero with crisis with other specified complication
HbS-beta zero with other specified complication
Sickle-cell beta zero with other specified complication
Use Additional Code: code to identify complications, such as:
cholelithiasis (K80.-)
priapism (N48.32)
D57.439Sickle-cell thalassemia beta zero with crisis, unspecified
HbS-beta zero with other specified complication
Sickle-cell beta zero with crisis unspecified
Sickle-cell thalassemia beta zero with (painful) crisis NOS
Sickle-cell thalassemia beta zero with (vaso-occlusive) pain NOS
D57.44Sickle-cell thalassemia beta plus without crisis
HbS-beta plus without crisis
Sickle-cell beta plus without crisis
D57.45Sickle-cell thalassemia beta plus with crisis
HbS-beta plus with crisis
Sickle-cell beta plus with crisis
D57.451Sickle-cell thalassemia beta plus with acute chest syndrome
HbS-beta plus with acute chest syndrome
Sickle-cell beta plus with acute chest syndrome
D57.452Sickle-cell thalassemia beta plus with splenic sequestration
HbS-beta plus with splenic sequestration
Sickle-cell beta plus with splenic sequestration
D57.453Sickle-cell thalassemia beta plus with cerebral vascular involvement
HbS-beta plus with cerebral vascular involvement
Sickle-cell beta plus with cerebral vascular involvement
Code Also: , if applicable cerebral infarction (I63.-)
D57.454Sickle-cell thalassemia beta plus with dactylitis
D57.458Sickle-cell thalassemia beta plus with crisis with other specified complication
HbS-beta plus with crisis with other specified complication
Sickle-cell beta plus with crisis with other specified complication
Use Additional Code: code to identify complications, such as:
cholelithiasis (K80.-)
priapism (N48.32)
D57.459Sickle-cell thalassemia beta plus with crisis, unspecified
HbS-beta plus with crisis with unspecified complication
Sickle-cell beta plus with crisis with unspecified complication
Sickle-cell thalassemia beta plus with (painful) crisis NOS
Sickle-cell thalassemia beta plus with (vaso-occlusive) pain NOS
D57.8Other sickle-cell disorders
Hb-SD disease
Hb-SE disease
D57.80Other sickle-cell disorders without crisis
D57.81Other sickle-cell disorders with crisis
D57.811Other sickle-cell disorders with acute chest syndrome
D57.812Other sickle-cell disorders with splenic sequestration
D57.813Other sickle-cell disorders with cerebral vascular involvement
Code Also: , if applicable: cerebral infarction (I63.-)
D57.814Other sickle-cell disorders with dactylitis
D57.818Other sickle-cell disorders with crisis with other specified complication
Use Additional Code: code to identify complications, such as:
cholelithiasis (K80.-)
priapism (N48.32)
D57.819Other sickle-cell disorders with crisis, unspecified
Other sickle-cell disorders with crisis NOS
Other sickle-cell disorders with (vaso-occlusive) pain NOS
D58Other hereditary hemolytic anemias
Excludes 1: hemolytic anemia of the newborn (P55.-)
D58.0Hereditary spherocytosis
Acholuric (familial) jaundice
Congenital (spherocytic) hemolytic icterus
Minkowski-Chauffard syndrome
D58.1Hereditary elliptocytosis
Elliptocytosis (congenital)
Ovalocytosis (congenital) (hereditary)
D58.2Other hemoglobinopathies
Abnormal hemoglobin NOS
Congenital Heinz body anemia
Hb-C disease
Hb-D disease
Hb-E disease
Hemoglobinopathy NOS
Unstable hemoglobin hemolytic disease
Excludes 1: familial polycythemia (D75.0)
Hb-M disease (D74.0)
hemoglobin E-beta thalassemia (D56.5)
hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
high-altitude polycythemia (D75.1)
methemoglobinemia (D74.-)
other hemoglobinopathies with thalassemia (D56.8)
D58.8Other specified hereditary hemolytic anemias
Stomatocytosis
D58.9Hereditary hemolytic anemia, unspecified
D59Acquired hemolytic anemia
D59.0Drug-induced autoimmune hemolytic anemia
Use Additional Code: code for adverse effect, if applicable, to identify drug (T36-T50) with fifth or sixth character 5)
D59.1Other autoimmune hemolytic anemias
Excludes 2: Evans syndrome (D69.41)
hemolytic disease of newborn (P55.-)
paroxysmal cold hemoglobinuria (D59.6)
D59.10Autoimmune hemolytic anemia, unspecified
D59.11Warm autoimmune hemolytic anemia
Warm type (primary) (secondary) (symptomatic) autoimmune hemolytic anemia
Warm type autoimmune hemolytic disease
D59.12Cold autoimmune hemolytic anemia
Chronic cold hemagglutinin disease
Cold agglutinin disease
Cold agglutinin hemoglobinuria
Cold type (primary) (secondary) (symptomatic) autoimmune hemolytic anemia
Cold type autoimmune hemolytic disease
D59.13Mixed type autoimmune hemolytic anemia
Mixed type autoimmune hemolytic disease
Mixed type, cold and warm, (primary) (secondary) (symptomatic) autoimmune hemolytic anemia
D59.19Other autoimmune hemolytic anemia
D59.2Drug-induced nonautoimmune hemolytic anemia
Drug-induced enzyme deficiency anemia
Use Additional Code: code for adverse effect, if applicable, to identify drug (T36-T50) with fifth or sixth character 5)
D59.3Hemolytic-uremic syndrome
Code Also: , if applicable, any associated:
acute kidney failure (N17.-)
chronic kidney disease (N18.-)
D59.30Hemolytic-uremic syndrome, unspecified
Hemolytic-uremic syndrome NOS
D59.31Infection-associated hemolytic-uremic syndrome
Shiga toxin-producing E. coli [STEC] related hemolytic uremic syndrome
Typical hemolytic uremic syndrome
Use Additional Code: code to identify associated infection, such as :
E. coli infection (B96.2-)
Human immunodeficiency virus [HIV] disease (B20)
Pneumococcal meningitis (G00.1)
Pneumococcal pneumonia (J13)
Sepsis due to Streptococcus pneumoniae (A40.3)
Shigella dysenteriae (A03.9)
Streptococcus pneumoniae as the cause of diseases classified elsewhere (B95.3)
D59.32Hereditary hemolytic-uremic syndrome
Atypical hemolytic uremic syndrome with an identified genetic cause
Code Also: , if applicable:
defects in the complement system (D84.1)
methylmalonic acidemia (E71.120)
D59.39Other hemolytic-uremic syndrome
Atypical (nongenetic) hemolytic uremic syndrome
Secondary hemolytic-uremic syndrome
Code First: , if applicable, any associated:
COVID-19 (U07.1)
complications of kidney transplant (T86.1-)
complications of heart transplant (T86.2-)
complications of liver transplant (T86.4-)
Code Also: , if applicable, any associated condition, such as:
hypertensive emergency (I16.1)
malignant neoplasm (C00-C96)
systemic lupus erythematosus (M32.-)
Use Additional Code: code, if applicable, for adverse effect to identify drug (T36-T50 with fifth or sixth character 5)
D59.4Other nonautoimmune hemolytic anemias
Mechanical hemolytic anemia
Microangiopathic hemolytic anemia
Toxic hemolytic anemia
D59.5Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
Excludes 1: hemoglobinuria NOS (R82.3)
D59.6Hemoglobinuria due to hemolysis from other external causes
Hemoglobinuria from exertion
March hemoglobinuria
Paroxysmal cold hemoglobinuria
Use Additional Code: code (Chapter 20) to identify external cause
Excludes 1: hemoglobinuria NOS (R82.3)
D59.8Other acquired hemolytic anemias
D59.9Acquired hemolytic anemia, unspecified
Idiopathic hemolytic anemia, chronic