16
ICD10 code of Fryns Syndrome and ICD9 code
What is the ICD10 code for Fryns Syndrome? And the ICD9 code for Fryns Syndrome?
Fryns Syndrome is a rare genetic disorder characterized by multiple congenital anomalies. Unfortunately, there is no specific ICD10 code assigned for Fryns Syndrome. However, it can be classified under Q87.8, which is a broader category for other specified congenital malformation syndromes. In terms of ICD9 code, Fryns Syndrome does not have a specific code either, but it can be classified under 759.89, which is a general code for other specified congenital anomalies.
Fryns Syndrome is a rare genetic disorder characterized by multiple congenital anomalies affecting various organ systems. Unfortunately, I cannot provide a specific ICD-10 code for Fryns Syndrome as it is not currently included in the ICD-10 classification system. However, I can provide you with some information about the condition and its manifestations.
Fryns Syndrome is typically diagnosed in newborns and is associated with a range of features including diaphragmatic hernia, facial abnormalities, limb defects, and underdeveloped lungs. Other common findings may include heart defects, brain abnormalities, and genitourinary malformations. The condition is often lethal, with a high mortality rate in affected individuals.
As for the ICD-9 code, it is important to note that the ICD-9 classification system has been replaced by ICD-10 since October 1, 2015. The ICD-9 code for Fryns Syndrome, if it had been included, would have likely fallen under the category of "congenital anomalies" or "syndromes associated with multiple malformations."
It is essential to consult with a healthcare professional or medical coding expert to obtain the most accurate and up-to-date information regarding classification and coding for Fryns Syndrome. They will be able to guide you in selecting the appropriate code based on the specific clinical features and documentation provided.
Fryns Syndrome is typically diagnosed in newborns and is associated with a range of features including diaphragmatic hernia, facial abnormalities, limb defects, and underdeveloped lungs. Other common findings may include heart defects, brain abnormalities, and genitourinary malformations. The condition is often lethal, with a high mortality rate in affected individuals.
As for the ICD-9 code, it is important to note that the ICD-9 classification system has been replaced by ICD-10 since October 1, 2015. The ICD-9 code for Fryns Syndrome, if it had been included, would have likely fallen under the category of "congenital anomalies" or "syndromes associated with multiple malformations."
It is essential to consult with a healthcare professional or medical coding expert to obtain the most accurate and up-to-date information regarding classification and coding for Fryns Syndrome. They will be able to guide you in selecting the appropriate code based on the specific clinical features and documentation provided.
Diseasemaps
