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ALL MEDICAL CODES IN CATEGORY Hemolytic anemias (D55-D59)
2025 ICD-10-CM code D59.31
Infection-associated hemolytic-uremic syndrome. This condition is characterized by the destruction of red blood cells, low platelet count, and kidney failure, typically associated with an infection.
2025 ICD-10-CM code D59.3
Hemolytic-uremic syndrome (HUS)
2025 ICD-10-CM code D55.0
Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency.
2025 ICD-10-CM code D58.0
Hereditary spherocytosis, a genetic blood disorder causing abnormal, sphere-shaped red blood cells and hemolytic anemia.
2025 ICD-10-CM code D57.44
Sickle-cell thalassemia beta plus without crisis.This condition combines sickle cell trait with beta-plus thalassemia, resulting in mild to moderate anemia but without a painful crisis.
2025 ICD-10-CM code D57.0
Hb-SS disease with crisis; Sickle cell disease with crisis.
2025 ICD-10-CM code D56.0
Alpha thalassemia encompasses various forms, including alpha thalassemia major, hemoglobin H disease, and hemoglobin H Constant Spring.It's characterized by a reduction in alpha-globin chains, leading to anemia.
2025 ICD-10-CM code D59.8
A type of anemia caused by the destruction of red blood cells faster than they are produced in the bone marrow.
2025 ICD-10-CM code D57.1
Sickle-cell disease without crisis. This is a genetic blood disorder characterized by sickle-shaped red blood cells and anemia, but without a vaso-occlusive crisis.
2025 ICD-10-CM code D57.09
Hb-SS disease with crisis with other specified complication. Use additional code to identify complications.
2025 ICD-10-CM code D57.20
Sickle-cell/Hb-C disease without crisis. This is a genetic blood disorder where red blood cells become hard, sticky, and C-shaped, leading to anemia but no vaso-occlusive crisis.
2025 ICD-10-CM code D57.4
Sickle-cell thalassemia. This is a genetic blood disorder where red blood cells become hard, sticky, and C-shaped, leading to anemia.
2025 ICD-10-CM code D56
Thalassemia is a genetic blood disorder characterized by a reduced amount of hemoglobin and red blood cells, leading to anemia.
2025 ICD-10-CM code D57.212
Sickle-cell/Hb-C disease with splenic sequestration. This is a complication of sickle-cell/Hb-C disease characterized by the rapid accumulation of sickle-shaped red blood cells in the spleen.
2025 ICD-10-CM code D59.6
Hemoglobinuria due to hemolysis from other external causes. This condition involves the destruction of red blood cells due to external factors, resulting in the release of hemoglobin and its excretion in urine.
2025 ICD-10-CM code D57.2
Sickle-cell/Hb-C disease. This is a type of sickle cell disease (SCD) where a patient inherits hemoglobin C, an abnormal gene leading to the formation of sickle-shaped red blood cells and anemia.
2025 ICD-10-CM code D57.219
Sickle-cell/Hb-C disease with crisis, unspecified. This condition involves painful vaso-occlusive crises due to the sickling of red blood cells in individuals with Hb-SC disease.
2025 ICD-10-CM code D59.9
فقر الدم الانحلالي المكتسب، غير محدد. تتضمن هذه الحالة التدمير المبكر لخلايا الدم الحمراء بسبب سبب غير معروف.
2025 ICD-10-CM code D59.9
获得性溶血性贫血，未具体说明。这种情况涉及由于未知原因而过早破坏红细胞。
2025 ICD-10-CM code D59.9
Anemia hemolítica adquirida, no especificada. Esta afección implica la destrucción prematura de los glóbulos rojos debido a una causa desconocida.
2025 ICD-10-CM code D59.9
Thiếu máu tán huyết mắc phải, không xác định. Tình trạng này liên quan đến sự phá hủy sớm các tế bào hồng cầu do một nguyên nhân không rõ.
Anémie hémolytique acquise, sans précision. Cette affection implique la destruction prématurée des globules rouges pour une cause inconnue.
2025 ICD-10-CM code D59.9
Приобретенная гемолитическая анемия неуточненная. Это состояние связано с преждевременным разрушением эритроцитов по неизвестной причине.
2025 ICD-10-CM code D59.9
상세불명의 후천성 용혈성 빈혈.이 질환은 원인 불명으로 인한 적혈구의 조기 파괴를 수반합니다.
2025 ICD-10-CM code D59.9
Erworbene hämolytische Anämie, nicht näher bezeichnet. Dieser Zustand beinhaltet die vorzeitige Zerstörung der roten Blutkörperchen aufgrund einer unbekannten Ursache.
Nakuha ang hemolithic anemia, hindi tinukoy. Ang kondisyong ito ay nagsasangkot ng napaaga na pagkasira ng mga pulang selula ng dugo dahil sa isang hindi kilalang sanhi
2025 ICD-10-CM code D59.31
Síndrome urémico hemolítico asociado a una infección. Esta afección se caracteriza por la destrucción de los glóbulos rojos, el recuento bajo de plaquetas y la insuficiencia renal, que generalmente se asocian a una infección.
2025 ICD-10-CM code D59.31
Hội chứng tan huyết - urê huyết liên quan đến nhiễm trùng. Tình trạng này được đặc trưng bởi sự phá hủy các tế bào hồng cầu, số lượng tiểu cầu thấp và suy thận, thường liên quan đến nhiễm trùng.
2025 ICD-10-CM code D57.819
A genetic blood disorder characterized by sickle-shaped red blood cells, leading to anemia and painful crises.This specific code indicates the presence of a crisis not otherwise specified (e.g., acute chest syndrome or splenic sequestration).
2025 ICD-10-CM code D57.41
Sickle-cell thalassemia with crisis. This is a type of sickle cell disease where a person inherits a sickle cell gene and a beta thalassemia gene, leading to abnormal red blood cells that can cause painful vaso-occlusive crises.
2025 ICD-10-CM code D56.2
Delta-beta thalassemia, also known as homozygous delta-beta thalassemia, is a rare blood disorder characterized by reduced or absent production of delta and beta globin chains.
2025 ICD-10-CM code D59.0
Drug-induced autoimmune hemolytic anemia. Use additional code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
2025 ICD-10-CM code D59
Acquired hemolytic anemia is a condition characterized by the premature destruction of red blood cells.
2025 ICD-10-CM code D59.2
Drug-induced nonautoimmune hemolytic anemia. This occurs when certain drug reactions damage red blood cells, usually destroying cell membranes.
2025 ICD-10-CM code D57.8
This code designates other sickle-cell disorders not otherwise specified, including Hb-SD disease and Hb-SE disease.
2025 ICD-10-CM code D58.1
Hereditary elliptocytosis is a genetic blood disorder characterized by oval or elliptical-shaped red blood cells (RBCs).It is a type of hereditary hemolytic anemia caused by genetic mutations in the RBC membrane.
2025 ICD-10-CM code D57.03
Hb-SS disease with cerebral vascular involvement. Code also, if applicable, cerebral infarction (I63.-).
2025 ICD-10-CM code D56.4
Hereditary persistence of fetal hemoglobin (HPFH).
2025 ICD-10-CM code D56.5
Hemoglobin E-beta thalassemia. This is a condition where there is a reduced amount of hemoglobin and red blood cells due to a combination of Hemoglobin E and beta thalassemia mutations.
2025 ICD-10-CM code D57.44
مرض الثلاسيميا المنجلية بيتا بلس بدون أزمة. تجمع هذه الحالة بين سمة الخلية المنجلية وثلاسيميا بيتا بلس، مما يؤدي إلى فقر الدم الخفيف إلى المتوسط ولكن دون أزمة مؤلمة.
2025 ICD-10-CM code D57.44
Thalassemia hồng cầu hình liềm beta cộng với không có khủng hoảng. Tình trạng này kết hợp đặc điểm hồng cầu hình liềm với bệnh thalassemia beta-plus, dẫn đến thiếu máu nhẹ đến trung bình nhưng không bị khủng hoảng đau đớn.
2025 ICD-10-CM code D57.44
Thalassémie drépanocytaire bêta plus sans crise. Cette affection associe un trait drépanocytaire à une thalassémie bêta-plus, entraînant une anémie légère à modérée mais sans crise douloureuse.
2025 ICD-10-CM code D57.44
Talasemia drepanocítica beta plus sin crisis. Esta afección combina el rasgo drepanocítico con la talasemia beta plus, lo que produce anemia leve a moderada, pero sin una crisis dolorosa.
2025 ICD-10-CM code D57.44
Серповидноклеточная талассемия бета плюс без криза. Это состояние сочетает в себе серповидноклеточную талассемию с талассемией бета-плюс, что приводит к анемии легкой или средней степени тяжести, но без болезненного криза.
겸상적혈구 지중해빈혈 베타 플러스 질환은 위기가 없습니다. 이 질환은 겸상적혈구 특성과 베타+지중해빈혈을 결합하여 경증에서 중등도의 빈혈을 유발하지만 고통스러운 위기는 아닙니다.
2025 ICD-10-CM code D57.44
Sichelzellen-Thalassämie Beta Plus ohne Krise. Diese Erkrankung kombiniert das Sichelzellenmerkmal mit der Beta-Plus-Thalassämie, was zu einer leichten bis mittelschweren Anämie führt, jedoch ohne eine schmerzhafte Krise.
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