ICD10 code of Robinow syndrome and ICD9 code

Robinow syndrome is a rare genetic disorder characterized by distinct facial features, skeletal abnormalities, and developmental delays. The International Classification of Diseases, 10th Revision (ICD-10), provides a specific code for Robinow syndrome, which is Q77.4. This code falls under the category of "Congenital malformation syndromes predominantly affecting facial appearance." It is important to note that the ICD-10 code is used internationally for documentation, billing, and statistical purposes.

On the other hand, the International Classification of Diseases, 9th Revision (ICD-9), which was replaced by ICD-10 in most countries, also had a code for Robinow syndrome. The ICD-9 code for this condition was 756.66, falling under the category of "Other congenital musculoskeletal anomalies." However, it is crucial to mention that ICD-9 codes are no longer actively used in many healthcare systems worldwide.

Robinow syndrome presents with various clinical features, including a "fetal face" appearance, with a broad forehead, widely spaced eyes, a flattened nasal bridge, and a small jaw. Additionally, affected individuals may exhibit short stature, limb abnormalities, and vertebral anomalies. The severity of symptoms can vary, even among individuals with the same genetic mutation.

In conclusion, the ICD-10 code for Robinow syndrome is Q77.4, while the ICD-9 code, which is now outdated, was 756.66. These codes help healthcare providers classify and document the condition for accurate diagnosis, treatment, and research purposes.

by Diseasemaps