The ICD10 code for Lenz Microphthalmia Syndrome is Q11.2. Unfortunately, there is no specific ICD9 code for this syndrome as it is a more recent classification system. Lenz Microphthalmia Syndrome is a rare genetic disorder characterized by small eyes (microphthalmia) and other associated abnormalities. It is important to consult with a healthcare professional for accurate diagnosis and appropriate treatment.
Lenz Microphthalmia Syndrome, also known as Lenz Syndrome, is a rare genetic disorder characterized by underdeveloped eyes (microphthalmia) or absent eyes (anophthalmia) and various other abnormalities affecting the facial features, limbs, and internal organs.
In the International Classification of Diseases, 10th Revision (ICD-10), Lenz Microphthalmia Syndrome is classified under Q11.2, which is the code for "Microphthalmos." This code specifically denotes the condition of microphthalmia, which is the primary manifestation of the syndrome.
In the previous version, ICD-9, Lenz Microphthalmia Syndrome was not specifically listed as a separate code. However, the condition could potentially be coded under 743.10, which represents "Microphthalmos, unspecified." It is important to note that ICD-9 codes are outdated, and healthcare providers have transitioned to using ICD-10 for improved accuracy and specificity in medical coding.
It is essential to consult with a healthcare professional or medical coder for accurate coding and classification of Lenz Microphthalmia Syndrome according to the latest ICD-10 guidelines.