Short answer · Medically reviewed summary · Last updated: 2026-05-08
Bilateral Renal Agenesis, also known as Potter sequence or Potter syndrome, is a rare congenital condition characterized by the complete absence of both kidneys at birth. While Bilateral Renal Agenesis is the precise anatomical description, medical literature often uses synonymous terms to describe the secondary physical features caused by the lack of amniotic fluid, such as pulmonary hypoplasia. What are the common synonyms for Bilateral Renal Agenesis? In medical records and historical literature, you may encounter several terms used to describe Bilateral Renal Agenesis.
Bilateral Renal Agenesis synonyms
Other names for Bilateral Renal Agenesis: synonyms, acronyms and related terms used by doctors and patients.
Bilateral Renal Agenesis, also known as Potter sequence or Potter syndrome, is a rare congenital condition characterized by the complete absence of both kidneys at birth. While Bilateral Renal Agenesis is the precise anatomical description, medical literature often uses synonymous terms to describe the secondary physical features caused by the lack of amniotic fluid, such as pulmonary hypoplasia.
What are the common synonyms for Bilateral Renal Agenesis?
In medical records and historical literature, you may encounter several terms used to describe Bilateral Renal Agenesis. The most common synonym is Potter syndrome, named after Dr. Edith Potter, who first described the clinical presentation. Other terms include bilateral renal agenesis sequence or, less frequently, classic Potter syndrome. While "Potter's facies" specifically refers to the facial features observed in these infants, it is sometimes used colloquially to describe the entire condition.
Why are there multiple names for this condition?
The variety of names for Bilateral Renal Agenesis stems from the distinction between the primary defect (the absence of kidneys) and the resulting cascade of physical effects. Historically, clinicians labeled the entire presentation as "Potter syndrome." However, modern medical nomenclature prefers the term Bilateral Renal Agenesis because it describes the specific anatomical pathology rather than just the secondary symptoms. This shift helps provide greater clarity in genetic counseling and diagnostic precision.
How is this condition classified in medical databases?
Standardized medical systems use specific codes to ensure consistent identification of Bilateral Renal Agenesis:
- OMIM (Online Mendelian Inheritance in Man): #191830 (Renal Agenesis, Bilateral)
- Orphanet: ORPHA:79476
- ICD-10: Q60.1 (Bilateral renal agenesis)
- ICD-11: LA00.00 (Bilateral renal agenesis)
Next steps
- Consult with a clinical geneticist to discuss recurrence risks for future pregnancies.
- Connect with the 19 members of the Bilateral Renal Agenesis community on DiseaseMaps.org for peer support.
- Request a referral to a perinatologist or a pediatric nephrologist if you are currently navigating a diagnosis.
Medical disclaimer: This content is for informational purposes only and does not constitute medical advice; always consult with your healthcare provider for clinical diagnosis and management.
References
- NIH Genetic and Rare Diseases Information Center (GARD): Renal agenesis, bilateral
- Orphanet: Bilateral renal agenesis
- OMIM: Renal Agenesis, Bilateral (#191830)
- National Library of Medicine: StatPearls - Potter Sequence
