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ICD10 code of Alveolar Capillary Dysplasia and ICD9 code

What is the ICD10 code for Alveolar Capillary Dysplasia? And the ICD9 code for Alveolar Capillary Dysplasia?

ICD9 and ICD10 codes of Alveolar Capillary Dysplasia

The ICD-10 code for Alveolar Capillary Dysplasia is Q33.4. In the ICD-9 coding system, there is no specific code for Alveolar Capillary Dysplasia. However, it may be classified under other related codes such as congenital anomalies of lung (748.3) or pulmonary hypoplasia (748.2). It is important to consult with a healthcare professional for accurate coding and diagnosis.
Alveolar Capillary Dysplasia (ACD) is a rare and severe developmental disorder affecting the lungs. It is characterized by abnormal development of the alveolar capillaries, which are the tiny blood vessels responsible for exchanging oxygen and carbon dioxide in the lungs. ACD is typically diagnosed in newborns or infants and is associated with severe respiratory distress and often leads to fatal outcomes.

In the International Classification of Diseases, 10th Revision (ICD-10), the specific code for Alveolar Capillary Dysplasia is Q33.4. This code falls under the category of "Congenital malformations of respiratory system" and further specifies the abnormality in the development of alveolar capillaries. It is important to note that ICD-10 codes are used globally for accurate and standardized classification of diseases, allowing healthcare professionals to effectively communicate diagnoses and facilitate research and data analysis.

In terms of the previous coding system, the ICD-9 code for Alveolar Capillary Dysplasia is 748.3. This code represents "Other anomalies of lung" and is found within the section of "Congenital anomalies of respiratory system." However, it is worth mentioning that ICD-9 codes have been replaced by ICD-10 codes since October 1, 2015, to provide a more detailed and comprehensive classification of diseases.

Overall, Alveolar Capillary Dysplasia is a serious condition with a specific ICD-10 code (Q33.4) that helps healthcare professionals accurately identify and document this rare lung disorder.
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