Leber Congenital Amaurosis (LCA) is a rare genetic disorder that affects the retina, leading to severe vision loss or blindness from birth or early infancy. The ICD-10 code for Leber Congenital Amaurosis is H35.50. In the previous coding system, ICD-9, the code for this condition was 362.74. These codes are used by healthcare professionals for accurate diagnosis and billing purposes.
Leber Congenital Amaurosis (LCA) is a rare inherited eye disorder that affects the retina, leading to severe vision loss in infancy or early childhood. In the International Classification of Diseases, 10th Revision (ICD-10), the specific code for Leber Congenital Amaurosis is H35.50. This code falls under the category of "Other Retinal Disorders" (H35) and indicates a bilateral involvement of the retina causing visual impairment.
In the previous version, the International Classification of Diseases, 9th Revision (ICD-9), Leber Congenital Amaurosis was classified under code 362.71. This code represented "Other Retinal Dystrophies" and denoted a similar condition with bilateral retinal involvement leading to visual impairment.
It is important to note that ICD codes are used for medical record-keeping, billing, and statistical purposes. They provide a standardized way to classify and document various health conditions. However, it is always advisable to consult with a healthcare professional for accurate diagnosis and appropriate treatment options for Leber Congenital Amaurosis.