Short answer · Medically reviewed summary · Last updated: 2023-07-10
Baller-Gerold Syndrome is a rare genetic disorder characterized by craniosynostosis (premature fusion of the skull bones) and radial aplasia/hypoplasia (underdevelopment or absence of the radius bone in the forearm). Although I am not a doctor, I can provide some information on the coding system used for medical diagnoses. In the International Classification of Diseases, Tenth Revision (ICD-10), Baller-Gerold Syndrome is classified under Q87.1, which falls under the category of "Congenital malformation syndromes predominantly affecting facial appearance." This code specifically denotes the syndrome involving craniosynostosis and radial aplasia/hypoplasia. On the other hand, the ICD-9 code for Baller-Gerold Syndrome would be 756.0, which is classified under "Congenital Anomalies of Skull and Face Bones." It is important to note that the ICD-9 code system has been replaced by ICD-10, which offers a more detailed and comprehensive classification of diseases and disorders. It is crucial to consult with a healthcare professional or a certified medical coder for accurate and up-to-date coding information.