ICD10 code of Singleton Merten syndrome and ICD9 code
What is the ICD10 code for Singleton Merten syndrome? And the ICD9 code for Singleton Merten syndrome?
The ICD-10 code for Singleton Merten syndrome is Q87.8. This code is used to classify this rare genetic disorder characterized by dental abnormalities, calcification of the aorta and heart valves, and skeletal abnormalities. Unfortunately, there is no specific ICD-9 code for Singleton Merten syndrome as it was replaced by the ICD-10 coding system. It is important to consult with a healthcare professional for accurate diagnosis and coding.
Singleton Merten syndrome is a rare genetic disorder characterized by a combination of dental abnormalities, skeletal abnormalities, and aortic calcification. It is an autosomal dominant disorder, which means that an affected individual has a 50% chance of passing the condition on to each of their children.
The ICD-10 code for Singleton Merten syndrome is Q87.8. This code falls under the category of "Other specified congenital malformation syndromes affecting multiple systems." The ICD-10 code system is used by healthcare professionals to classify and code diagnoses, symptoms, and procedures for billing, statistical, and research purposes.
Unfortunately, there is no specific ICD-9 code for Singleton Merten syndrome. The ICD-9 code system, which was used prior to the implementation of ICD-10, does not have a direct equivalent for this particular syndrome. However, healthcare providers may have used a combination of codes to describe the individual symptoms and abnormalities associated with Singleton Merten syndrome.
It is important to note that the transition from ICD-9 to ICD-10 occurred on October 1, 2015, and healthcare providers are now required to use the ICD-10 code set for all diagnoses and procedures. The ICD-10 code Q87.8 should be used to identify cases of Singleton Merten syndrome.
Singleton Merten syndrome is characterized by a range of symptoms and abnormalities. Dental abnormalities may include early loss of primary teeth, delayed eruption of permanent teeth, and abnormal tooth enamel. Skeletal abnormalities can involve progressive thinning of the bones (osteoporosis), joint laxity, and abnormal bone development. Aortic calcification, which is the abnormal accumulation of calcium in the aortic valve and walls, can lead to heart problems such as aortic stenosis or aortic regurgitation.
Due to the rarity of Singleton Merten syndrome, there is limited information available regarding its underlying genetic cause and specific treatment options. Management of the condition typically involves a multidisciplinary approach, with healthcare professionals addressing the individual symptoms and complications that arise. Regular monitoring of dental, skeletal, and cardiovascular health is essential to detect and manage any issues that may arise.
In conclusion, the ICD-10 code for Singleton Merten syndrome is Q87.8, while there is no specific ICD-9 code for this syndrome. Singleton Merten syndrome is a rare genetic disorder characterized by dental abnormalities, skeletal abnormalities, and aortic calcification. Healthcare providers use these codes to classify and code diagnoses for billing, statistical, and research purposes.
