Wildervanck Syndrome is a rare genetic disorder characterized by a combination of Klippel-Feil anomaly, hearing loss, and Duane syndrome. It is typically seen in females during adolescence. The ICD-10 code for Wildervanck Syndrome is Q87.8. Unfortunately, there is no specific ICD-9 code for this syndrome as it was replaced by ICD-10 in 2015.
Wildervanck Syndrome, also known as cervico-oculo-acoustic syndrome, is a rare disorder characterized by a triad of symptoms including Klippel-Feil anomaly (congenital fusion of cervical vertebrae), hearing loss, and Duane syndrome (a type of eye movement disorder). While ICD10 codes are used to classify diseases and medical conditions, ICD9 codes have been replaced by ICD10 codes since October 1, 2015. Therefore, there is no specific ICD9 code for Wildervanck Syndrome. In the ICD10 coding system, Wildervanck Syndrome is classified under Q87.0, which is the code for Congenital Malformation Syndromes Predominantly Associated with Short Stature. It is important to note that accurate coding should be performed by healthcare professionals based on the specific clinical presentation of the patient.