Keratitis Ichthyosis Deafness (KID) Syndrome is a rare genetic disorder characterized by the presence of various symptoms including inflammation of the cornea (keratitis), dry and scaly skin (ichthyosis), and hearing loss (deafness). The ICD-10 code for KID Syndrome is Q87.8, which falls under the category of "Other specified congenital malformation syndromes predominantly associated with short stature."
In the previous ICD-9 coding system, KID Syndrome did not have a specific code. However, the closest code that could be used to describe the condition is 757.39, which falls under the category of "Other specified anomalies of skin." It is important to note that the transition from ICD-9 to ICD-10 coding systems has allowed for more specific and accurate coding of various medical conditions, including KID Syndrome.
It is always recommended to consult with a healthcare professional or medical coder for accurate coding and billing purposes.
Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2023-07-10
Medical disclaimer:
This information does not substitute professional medical advice. Always consult your doctor before making health decisions.