ICD10 code of Mowat-Wilson syndrome and ICD9 code

Mowat-Wilson syndrome is a rare genetic disorder characterized by multiple physical and developmental abnormalities. The specific ICD-10 code assigned to this condition is Q93.8. The ICD-10 code system is a standardized classification system used by healthcare professionals to document and code various diagnoses.

In terms of the ICD-9 code, this classification system was replaced by ICD-10 on October 1, 2015, in most countries. However, for the sake of completeness, the corresponding ICD-9 code for Mowat-Wilson syndrome was 758.39. The ICD-9 code system was used prior to the implementation of ICD-10 and allowed medical professionals to classify and report diagnoses for billing and statistical purposes.

Mowat-Wilson syndrome is caused by mutations or deletions in the ZEB2 gene, which plays a critical role in embryonic development. Common features of this syndrome include distinctive facial features, intellectual disability, delayed growth, and various congenital abnormalities affecting the heart, urinary tract, and gastrointestinal system.

It is important to note that the information provided is for general knowledge purposes only and should not be used for diagnostic or treatment purposes. If you suspect that you or someone you know may have Mowat-Wilson syndrome, it is essential to consult with a qualified healthcare professional for a comprehensive evaluation and accurate diagnosis.

by Diseasemaps