The ICD-10 code for SHORT syndrome is Q87.1. SHORT syndrome is a rare genetic disorder characterized by short stature, hyperextensibility of joints, hernias, ocular depression, Rieger anomaly, and teething delay. It is caused by mutations in the PIK3R1 gene. Unfortunately, there is no specific ICD-9 code for SHORT syndrome as it was replaced by ICD-10 codes. It is important to consult a healthcare professional for accurate diagnosis and appropriate management of this condition.
SHORT syndrome is a rare genetic disorder characterized by short stature, hyperextensibility of joints, ocular depression, Rieger anomaly, and teething delay. However, it is important to note that the term "SHORT syndrome" is not recognized in the International Classification of Diseases, Tenth Revision (ICD-10).
To accurately assign an ICD-10 code for the symptoms associated with SHORT syndrome, it would be necessary to identify the specific manifestations present in each patient. For example, short stature could be coded using Q77.4 (Other osteochondrodysplasias with short stature), while Rieger anomaly might be coded as Q13.89 (Other specified congenital malformations of anterior segment of eye). Additionally, any other accompanying symptoms or conditions would require their respective codes.
Regarding the ICD-9 code, it is important to note that ICD-9 has been replaced by ICD-10 since October 1, 2015, as the official coding system. However, for historical reference, the ICD-9 code for SHORT syndrome would have been 759.89 (Other specified congenital anomalies) or other more specific codes depending on the individual symptoms present.
It is always recommended to consult a healthcare professional or a certified medical coder for accurate coding and documentation purposes.