ICD10 code of Bilateral Renal Agenesis and ICD9 code

Bilateral renal agenesis, also known as bilateral renal hypoplasia or Potter syndrome type I, is a rare congenital condition characterized by the absence or underdevelopment of both kidneys. This condition occurs when the kidneys fail to form during fetal development, leading to a variety of complications such as low amniotic fluid levels, abnormal lung development, and potentially life-threatening complications after birth.

In the International Classification of Diseases, Tenth Revision (ICD-10), bilateral renal agenesis is assigned the code Q60.1. The "Q" signifies that it is a congenital malformation, while "60" represents the chapter on congenital malformations, deformations, and chromosomal abnormalities. The ".1" further specifies that it refers to bilateral renal agenesis specifically.

In the previous edition of the classification system, the Ninth Revision (ICD-9), bilateral renal agenesis was coded as 753.0. The "753" category in ICD-9 pertains to congenital anomalies of the genitourinary system, and the ".0" indicates bilateral renal agenesis.

It is important to note that the ICD codes are used for medical classification and billing purposes, helping healthcare providers and insurance companies identify and categorize specific conditions. These codes facilitate accurate documentation, research, and statistical analysis of various health conditions, including bilateral renal agenesis.

It is crucial for individuals affected by or working with patients with bilateral renal agenesis to consult medical professionals for accurate diagnosis, treatment, and management of this complex condition.

by Diseasemaps