The ICD-10 code for Winchester Syndrome is M14.8. Winchester Syndrome is a rare genetic disorder characterized by skeletal abnormalities, joint stiffness, and progressive joint destruction. It is also known as hereditary arthro-ophthalmopathy. Unfortunately, there is no specific ICD-9 code for Winchester Syndrome as it was replaced by ICD-10 in 2015. It is important to consult with a healthcare professional for accurate diagnosis and appropriate treatment.
Winchester Syndrome, also known as Torg-Winchester Syndrome, is an extremely rare genetic disorder characterized by progressive joint and bone abnormalities. This condition falls under the broader category of skeletal dysplasias. Unfortunately, due to the limited availability of information, there is no specific ICD-10 code dedicated solely to Winchester Syndrome.
However, certain aspects of Winchester Syndrome may be classified using more general ICD-10 codes. For instance, the joint abnormalities associated with this condition might be classified using codes such as M25.5 (joint instability) or M24.8 (other specific joint derangements). Additionally, the bone abnormalities could potentially be classified using codes like Q78.9 (osteochondrodysplasia, unspecified) or M89.9 (disorder of bone, unspecified).
In terms of ICD-9 coding, Winchester Syndrome does not have a specific code either. Similar to the ICD-10 classification, related symptoms or manifestations may be coded using more general codes. For example, joint instability could be coded as 718.9 (unspecified derangement of joint). Similarly, bone abnormalities might be classified as 756.9 (unspecified congenital anomaly of bone).
Remember, it is always essential to consult with a healthcare professional or medical coder to ensure accurate coding and documentation of any specific medical condition, especially when dealing with rare disorders like Winchester Syndrome.