The ICD-10 code for Ectrodactyly is Q71.8, which falls under the category of "Other Congenital Malformations of Limbs." Ectrodactyly is a rare genetic disorder characterized by the absence or malformation of one or more fingers or toes. Unfortunately, ICD-9 codes are no longer used as of October 1, 2015, and have been replaced by ICD-10 codes for medical classification purposes.
Ectrodactyly, also known as split hand/split foot malformation, is a rare congenital condition characterized by the absence or malformation of digits in the hands and/or feet. It is typically inherited as an autosomal dominant trait, although sporadic cases can occur.
In the International Classification of Diseases, 10th Revision (ICD-10), the specific code for ectrodactyly is Q71.8. This code falls under the broader category of "Other specified congenital malformations of limb(s)". The ICD-10 provides a standardized system for classifying and coding diseases, disorders, and other health conditions to facilitate accurate medical record-keeping, statistical analysis, and reimbursement purposes.
In the previous version, the International Classification of Diseases, 9th Revision (ICD-9), ectrodactyly was classified under code 755.59. The ICD-9 system was used until the transition to ICD-10 was implemented in most countries.
It is important to note that the ICD codes are used by healthcare professionals and researchers worldwide to document and classify various conditions. These codes allow for improved communication, research, and analysis of health data. However, it is always recommended to consult with a healthcare professional for a comprehensive diagnosis and appropriate treatment options for any medical condition.