Short answer · Medically reviewed summary · Last updated: 2026-05-08
Bilateral Renal Agenesis, historically known as Potter sequence, is classified under ICD-10 code Q60.1 (Bilateral renal agenesis) and ICD-9 code 753.0 (Renal agenesis and dysgenesis). These codes are used by medical professionals to document this rare congenital condition characterized by the complete absence of both kidneys at birth. What is Bilateral Renal Agenesis? Bilateral Renal Agenesis is a rare, life-limiting condition where a fetus fails to develop both kidneys in utero.
ICD10 code of Bilateral Renal Agenesis and ICD9 code
ICD-10 and ICD-9 codes for Bilateral Renal Agenesis, with classification details for clinicians, coders and patients.
Bilateral Renal Agenesis, historically known as Potter sequence, is classified under ICD-10 code Q60.1 (Bilateral renal agenesis) and ICD-9 code 753.0 (Renal agenesis and dysgenesis). These codes are used by medical professionals to document this rare congenital condition characterized by the complete absence of both kidneys at birth.
What is Bilateral Renal Agenesis?
Bilateral Renal Agenesis is a rare, life-limiting condition where a fetus fails to develop both kidneys in utero. Because the kidneys are responsible for producing amniotic fluid, their absence leads to oligohydramnios (low amniotic fluid), which subsequently causes pulmonary hypoplasia and characteristic facial features. With 19 members currently sharing their experiences on DiseaseMaps.org, we recognize the profound emotional impact this diagnosis has on families navigating such a complex medical journey.
How is the diagnosis confirmed?
Diagnosis of Bilateral Renal Agenesis is typically made via prenatal ultrasound, which reveals the absence of renal tissue and a severely reduced amniotic fluid volume. Following birth, clinical confirmation involves a physical examination and imaging studies to identify the specific anatomical findings associated with Bilateral Renal Agenesis. Genetic counseling is strongly recommended, as this condition may occur sporadically or as part of a larger genetic syndrome.
What are the clinical implications of this condition?
The clinical management of Bilateral Renal Agenesis is centered on the severity of the associated pulmonary hypoplasia. Key clinical considerations include:
- Pulmonary Hypoplasia: The primary cause of respiratory failure in newborns with Bilateral Renal Agenesis.
- Potter Sequence: A collection of physical findings including low-set ears, a beaked nose, and limb abnormalities resulting from fetal compression.
- Genetic Evaluation: Assessment for associated syndromes, such as Branchio-Oto-Renal (BOR) syndrome or other chromosomal anomalies.
- Multidisciplinary Care: Coordination between neonatologists, geneticists, and palliative care teams to provide comprehensive support.
Next steps
- Consult with a board-certified clinical geneticist to discuss recurrence risks for future pregnancies.
- Connect with the DiseaseMaps.org community to share experiences and find support from others who have navigated a diagnosis of Bilateral Renal Agenesis.
- Seek specialized grief and trauma counseling, as the emotional burden of Bilateral Renal Agenesis is significant for parents and caregivers.
Medical disclaimer: This information is for educational purposes only and does not constitute professional medical advice, diagnosis, or treatment; always seek the advice of a physician regarding a medical condition.
References
- NIH Genetic and Rare Diseases Information Center (GARD): Bilateral Renal Agenesis
- Orphanet: Renal Agenesis, Bilateral (ORPHA:3146)
- OMIM (Online Mendelian Inheritance in Man): Renal Agenesis, Bilateral (#266900)
- ICD-10 Data: Q60.1 Bilateral renal agenesis
