Upgrade for detailed insurance, legislation, and other documents analytics for individual cases; real-time analysis of the datasets from your EHR, CRM, ERP, or other software; and more Enterprise Features.
ALL MEDICAL CODES IN CATEGORY Coagulation defects, purpura and other hemorrhagic conditions
2025 ICD-10-CM code D68.0
Von Willebrand disease. This is a bleeding disorder characterized by a deficiency or dysfunction of von Willebrand factor (VWF), a protein crucial for blood clotting.
2025 ICD-10-CM code D69.4
Other primary thrombocytopenia. This code excludes transient neonatal thrombocytopenia (P61.0) and Wiskott-Aldrich syndrome (D82.0).
2025 ICD-10-CM code D68.00
Von Willebrand disease, unspecified.
2025 ICD-10-CM code D69.0
Allergic purpura is a condition causing inflammation of small blood vessels (capillaries) in the skin, kidneys, and intestines, often developing in children after an infection.
2025 ICD-10-CM code D65
Disseminated intravascular coagulation (DIC), also known as consumption coagulopathy or defibrination syndrome.
2025 ICD-10-CM code D69.51
Posttransfusion purpura (PTP) is an adverse reaction to blood or platelet transfusion, causing sudden thrombocytopenia about 7-10 days post-transfusion.
2025 ICD-10-CM code D69.49
Other primary thrombocytopenia. This condition involves a deficiency of platelets in the blood, not categorized elsewhere, leading to abnormal bleeding.
2025 ICD-10-CM code D68.59
Other primary thrombophilia. This is a blood disorder that increases the risk of blood clots.
2025 ICD-10-CM code D69.42
Congenital and hereditary thrombocytopenia purpura is an inherited disorder characterized by abnormal platelet function leading to excessive bleeding.
2025 ICD-10-CM code D68.69
This code represents a thrombophilia, a condition that increases the risk of blood clots, that is not otherwise specified.
2025 ICD-10-CM code D68.312
Antiphospholipid antibody with hemorrhagic disorder.This condition involves bleeding due to the presence of antiphospholipid antibodies.
2025 ICD-10-CM code D68.5
Primary thrombophilia. Increased tendency for blood clotting.
2025 ICD-10-CM code D68.52
Prothrombin gene mutation, a disorder causing increased blood clotting risk.
2025 ICD-10-CM code D68.04
Acquired von Willebrand disease, also known as Acquired von Willebrand syndrome.
2025 ICD-10-CM code D69.8
Otras afecciones hemorrágicas especificadas.Incluye la fragilidad capilar (hereditaria) y la pseudohemofilia vascular.
2025 ICD-10-CM code D69.8
حالات نزفية محددة أخرى. تشمل هشاشة الشعيرات الدموية (الوراثية) والهيموفيليا الكاذبة الوعائية.
2025 ICD-10-CM code D69.8
其他特定的出血性疾病。包括毛细血管脆弱性（遗传）和血管性假血友病。
2025 ICD-10-CM code D69.8
Другие уточненные геморрагические состояния. Включают хрупкость капилляров (наследственную) и сосудистую псевдогемофилию.
2025 ICD-10-CM code D69.8
Autres affections hémorragiques précisées. Comprend la fragilité capillaire (héréditaire) et la pseudohémophilie vasculaire.
2025 ICD-10-CM code D69.8
Các tình trạng xuất huyết được chỉ định khác.Bao gồm sự mong manh của mao mạch (di truyền) và pseudohemophilia mạch máu.
2025 ICD-10-CM code D69.8
Andere näher bezeichnete hämorrhagische Erkrankungen. Beinhaltet kapillare Fragilität (erblich) und vaskuläre Pseudohämophilie.
2025 ICD-10-CM code D69.8
기타 특정 출혈성 질환. 모세 혈관 취약성 (유전성) 및 혈관 가성 혈우병이 포함됩니다.
2025 ICD-10-CM code D69.8
Iba pang tinukoy na mga kondisyong hemorrhagiko.Kasama sa kapilyar na kahinaan (namana) at vascular pseudohemophilia.
2025 ICD-10-CM code D69.5
Pangalawang thrombocytopenia.Isang kondisyon na nailalarawan ng isang mababang bilang ng platelet na nagreresulta mula sa isa pang nakapailalim na medikal na isyu.
2025 ICD-10-CM code D69.1
Mga kuwalitibong depekto sa platelet, kabilang ang Bernard-Soulier syndrome, Glanzmann-'s disease, Grey platelet syndrome, Thromboasthenia, at Thrombocytopathy.
2025 ICD-10-CM code D69.1
Anomalies plaquettaires qualitatives, y compris le syndrome de Bernard-Soulier, la maladie de Glanzmann, le syndrome des plaquettes grises, la thromboasthénie et la thrombocytopathie.
2025 ICD-10-CM code D69.42
Die angeborene und erbliche Thrombozytopenie Purpura ist eine Erbkrankheit, die durch eine abnormale Blutplättchenfunktion gekennzeichnet ist, die zu übermäßigen Blutungen führt.
2025 ICD-10-CM code D69.42
先天性和遗传性血小板减少症紫癜是一种遗传性疾病，其特征是血小板功能异常导致出血过多。
2025 ICD-10-CM code D69.2
Другая нетромбоцитопеническая пурпура. Это состояние характеризуется кровотечением под кожей, вызывающим появление красных или фиолетовых пятен без снижения количества тромбоцитов.
2025 ICD-10-CM code D69.6
Isang kondisyon na nailalarawan ng isang mababang bilang ng platelet, mahalaga para sa pagbuot ng dugo. Ang sanhi ay hindi tinukoy.
2025 ICD-10-CM code D69.6
Ein Zustand, der durch eine niedrige Thrombozytenzahl gekennzeichnet ist, die für die Blutgerinnung unerlässlich ist. Die Ursache ist nicht spezifiziert.
2025 ICD-10-CM code D69.6
Một tình trạng đặc trưng bởi số lượng tiểu cầu thấp, cần thiết cho quá trình đông máu.Nguyên nhân không xác định.
2025 ICD-10-CM code D69.6
حالة تتميز بانخفاض عدد الصفائح الدموية، وهي ضرورية لتخثر الدم. السبب غير محدد.
2025 ICD-10-CM code D69.6
Состояние, характеризующееся низким уровнем тромбоцитов, необходимых для свертывания крови. Причина не установлена.
2025 ICD-10-CM code D69.51
La púrpura postrasfusional (<a href="../medical-coding/reference/PTP" target="_blank" title="Medical Code PTP 2025">PTP</a>) es una reacción adversa a la transfusión de sangre o plaquetas que causa trombocitopenia súbita entre 7 y 10 días después de la transfusión.
2025 ICD-10-CM code D69.6
Affection caractérisée par une faible numération plaquettaire, essentielle à la coagulation du sang. La cause n'est pas précisée.
2025 ICD-10-CM code D69.5
Trombocitopenia secundaria. Afección caracterizada por un recuento bajo de plaquetas como resultado de otro problema médico subyacente.
2025 ICD-10-CM code D69.42
La púrpura trombocitopénica congénita y hereditaria es un trastorno hereditario caracterizado por una función plaquetaria anormal que conduce a un sangrado excesivo.
2025 ICD-10-CM code D69.42
فرفرية نقص الصفيحات الخلقية والوراثية هي اضطراب وراثي يتميز بوظيفة الصفائح الدموية غير الطبيعية التي تؤدي إلى نزيف مفرط.
2025 ICD-10-CM code D69.51
Ban xuất huyết sau truyền máu (<a href="../medical-coding/reference/PTP" target="_blank" title="Medical Code PTP 2025">PTP</a>) là một phản ứng bất lợi đối với truyền máu hoặc tiểu cầu, gây giảm tiểu cầu đột ngột khoảng 7-10 ngày sau khi truyền máu.
2025 ICD-10-CM code D69.51
Purpura nach Transfusion (<a href="../medical-coding/reference/PTP" target="_blank" title="Medical Code PTP 2025">PTP</a>) ist eine Nebenwirkung einer Blut- oder Blutplättchentransfusion, die etwa 7 bis 10 Tage nach der Transfusion zu einer plötzlichen Thrombozytopenie führt.
2025 ICD-10-CM code D69.51
수혈 후 자반병 (<a href="../medical-coding/reference/PTP" target="_blank" title="Medical Code PTP 2025">PTP</a>) 은 혈액 또는 혈소판 수혈에 대한 부작용으로 수혈 후 약 7-10일 후에 갑작스러운 혈소판 감소증을 유발합니다.
2025 ICD-10-CM code D69.51
Le purpura post-transfusionnel (<a href="../medical-coding/reference/PTP" target="_blank" title="Medical Code PTP 2025">PTP</a>) est un effet indésirable à la transfusion de sang ou de plaquettes, provoquant une thrombocytopénie soudaine environ 7 à 10 jours après la transfusion.
2025 ICD-10-CM code D69.51
Посттрансфузионная пурпура (<a href="../medical-coding/reference/PTP" target="_blank" title="Medical Code PTP 2025">PTP</a>) — это побочная реакция на переливание крови или тромбоцитов, вызывающая внезапную тромбоцитопению примерно через 7-10 дней после переливания крови.
Вторичная тромбоцитопения. Состояние, характеризующееся низким уровнем тромбоцитов в результате другой основной медицинской проблемы.
2025 ICD-10-CM code D69.51
فرفرية ما بعد نقل الدم (<a href="../medical-coding/reference/PTP" target="_blank" title="Medical Code PTP 2025">PTP</a>) هي رد فعل سلبي لنقل الدم أو الصفائح الدموية، مما يتسبب في نقص الصفيحات المفاجئ بعد حوالي 7-10 أيام من نقل الدم.
2025 ICD-10-CM code D69.5
Giảm tiểu cầu thứ phát. Một tình trạng đặc trưng bởi số lượng tiểu cầu thấp do một vấn đề y tế tiềm ẩn khác.
2025 ICD-10-CM code D69.5
نقص الصفيحات الثانوي. حالة تتميز بانخفاض عدد الصفائح الدموية الناتج عن مشكلة طبية أساسية أخرى.
2025 ICD-10-CM code D69.1
Defectos plaquetarios cualitativos, como el síndrome de Bernard-Soulier, la enfermedad de Glanzmann, el síndrome de las plaquetas grises, la tromboastenia y la trombocitopatía.
Continue with Personal Account
Thank you for exploring iFrame ♥ Please subscribe for unlimited access to our top-tier AI model, which directly supports our dedicated knowledge creators maintaining an ad-free internet experience.