Campomelic Dysplasia (CMD) is a rare genetic disorder characterized by skeletal and developmental abnormalities. The ICD-10 code for Campomelic Dysplasia is Q87.1. Unfortunately, there is no specific ICD-9 code for Campomelic Dysplasia as it is an outdated coding system. It is important to consult with a healthcare professional for accurate diagnosis and coding information.
Campomelic dysplasia (CMD) is a rare genetic disorder characterized by skeletal abnormalities and other developmental issues. The International Classification of Diseases, 10th Revision (ICD-10) code for Campomelic Dysplasia is Q87.1. This code falls under the category of "Congenital malformation syndromes predominantly affecting facial appearance," specifically disorders of bone development and skeletal dysplasias.
In contrast, the International Classification of Diseases, 9th Revision (ICD-9) code for Campomelic Dysplasia is 758.89. This code is found in the section for "Other congenital anomalies of the musculoskeletal system." It is important to note that ICD-9 codes have been replaced by ICD-10 codes, which provide more detailed and specific classification of diseases and conditions.
Campomelic Dysplasia is a serious condition that affects multiple body systems. It is typically characterized by bowed long bones, a small chest, and a distinctive facial appearance. Additionally, individuals with CMD may have underdeveloped lungs, heart defects, and genital abnormalities. The severity of symptoms can vary widely, and affected individuals often require ongoing medical care and support.
It is essential for healthcare professionals to accurately code and document conditions like Campomelic Dysplasia using the appropriate ICD-10 code. This ensures proper tracking of the prevalence of the disorder and facilitates appropriate treatment and management strategies for affected individuals.